510 k database | Search the Releasable 510(k) Database

Keyword	CPC	PCC	Volume	Score	Length of keyword
510 k database	1.27	0.3	9975	21	14
510	1.9	0.8	6061	65	3
k	0.76	0.9	5779	87	1
database	0.42	0.2	8229	32	8

Keyword	CPC	PCC	Volume	Score
510 k database	1.01	0.7	2138	31
510 k database fda	1.87	1	803	1
510 k database search	1.15	0.8	387	76
510 k database searchable	0.57	0.1	8141	23
510 k database access	0.41	0.7	5147	6
510 k database lookup	0.01	0.6	3528	46
510 k database lateral flow assay covid 19	1.48	0.2	1469	99
fda releasable 510 k database	0.29	0.1	4836	2
fda 510 k approval database	1.4	0.1	5623	13
fda searchable 510 k database	1.54	0.6	4143	22
fda 510 k database search	0.85	0.5	2722	10
us fda 510 k database	0.66	0.3	2048	58
fda 510 k premarket notification database	0.94	0.4	7977	19

Search Results related to 510 k database on Search Engine

Search the Releasable 510(k) Database | FDA
fda.gov

https://www.fda.gov/medical-devices/510k-clearances/search-releasable-510k-database

WEBYou can search the releasable 510 (k) database by Panel, 510 (k) number, Product code or Device name. A search query will produce information from the database in the following format:...

DA: 24 PA: 15 MOZ Rank: 69 Up or Down: Up

510(k) Premarket Notification - Food and Drug Administration
fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm

WEB4 days ago · Medical Devices. Databases. A 510 (K) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a...

DA: 95 PA: 46 MOZ Rank: 47 Up or Down: Up

Premarket Notification 510(k) | FDA
fda.gov

https://www.fda.gov/medical-devices/premarket-submissions-selecting-and-preparing-correct-submission/premarket-notification-510k

WEBOct 3, 2022 · A 510 (k) is a premarket submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent, to a legally marketed device (section... database

database

DA: 36 PA: 73 MOZ Rank: 24 Up or Down: Up

510(k) Clearances | FDA - U.S. Food and Drug Administration
fda.gov

https://www.fda.gov/medical-devices/device-approvals-and-clearances/510k-clearances

WEBNov 6, 2023 · Browse and Search for 510(k) Clearances. Search the 510(k) Premarket Notification database. Browse for Clearances by Year. 510(k) Devices Cleared in 2023; 510(k) Devices Cleared...

DA: 65 PA: 4 MOZ Rank: 94 Up or Down: Up

510(K) Premarket Notification - Food and Drug Administration
fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/TextResults.cfm

WEB510(K) Number. Decision Date. sem scanner (model 200) Bruin Biometrics, LLC den170021: 12/20/2018: single size tendon spacer: MEDIST INTERNATIONAL k000019: 03/29/2000: next step powder free latex examination gloves contains 50 mcgm or less of total water extractable protein per gram: ANSELL PERRY ... database

database

DA: 36 PA: 29 MOZ Rank: 45 Up or Down: Up

510 (k) Clearances - Food and Drug Administration
fda.gov

https://open.fda.gov/data/510k/

WEBA 510 (k) is a premarketing submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent (SE), to a legally marketed device... database

database

DA: 81 PA: 31 MOZ Rank: 69 Up or Down: Up

Device 510(k) Overview - Food and Drug Administration
fda.gov

https://open.fda.gov/apis/device/510k/

WEBKey Facts. Source of the data: 510 (k) Clearances. Changes to the source data: openFDA annotates the original records with special fields and converts the data into JSON, which is a widely used... database

database

DA: 18 PA: 65 MOZ Rank: 38 Up or Down: Up

510(k) Clearances | FDA - U.S. Food and Drug Administration
fda.gov

https://www.fda.gov/medical-devices/device-approvals-denials-and-clearances/510k-clearances

WEBAug 31, 2021 · Search the Releasable 510(k) Database; 510(k) Devices Cleared in 2023; 510(k) Devices Cleared in 2022; 510(k) Devices Cleared in 2021; 510(k) Devices Cleared in 2020;...

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FDA 510(k) Explained: A Basic Guide to Premarket Notification
thefdagroup.com

https://www.thefdagroup.com/blog/510k-explained

WEBMar 23, 2023 · The 510 (k) regulatory pathway is a submission process that medical device manufacturers use to get clearance from the FDA to market an eligible product in the U.S.

DA: 69 PA: 79 MOZ Rank: 18 Up or Down: Up

FDA Premarket Notification 510(k) | NBER
nber.org

https://www.nber.org/research/data/fda-premarket-notification-510k

WEBPremarket Notification 510 (k) searchable database. CFR search engine. The complete FDA Premarket Notification database is offered here in SAS, Stata, and CSV formats to make the whole database a bit easier to use. Updates and changes. Pre-Stata13 had a string length limit of 244 characters.

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