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

Keyword	CPC	PCC	Volume	Score	Length of keyword
fda 510 k database	1.8	1	450	38	18
fda	0.77	0.7	8904	27	3
510	1.45	0.3	4169	15	3
k	1.89	0.3	5769	88	1
database	1.72	0.7	794	46	8

Keyword	CPC	PCC	Volume	Score
fda 510 k database	1.58	0.1	9807	31

Search Results related to fda 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...

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

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

Web3 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: 76 PA: 97 MOZ Rank: 86

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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Medical Device Databases | FDA
fda.gov

https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/medical-device-databases

WebThis database of releasable 510(k)s can be searched by 510(k) number, applicant, device name or FDA product code. Summaries of safety and effectiveness information is available via...

DA: 66 PA: 71 MOZ Rank: 61

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 · Search the 510(k) Premarket Notification database. Browse for Clearances by Year. 510(k) Devices Cleared in 2023; 510(k) Devices Cleared in 2022; 510(k) Devices Cleared in 2021

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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...

DA: 69 PA: 24 MOZ Rank: 18

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 ... U.S. Food and Drug Administration. 10903 New Hampshire Avenue Silver Spring, MD 20993 Ph. 1-888-INFO-FDA (1-888-463-6332) Contact FDA. For Government; For Press;

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510(k) Submission Process | FDA
fda.gov

https://www.fda.gov/medical-devices/premarket-notification-510k/510k-submission-process

WebStarting October 1, 2023, all 510 (k) submissions, unless exempted (as described in Section VI.A of the final guidance, Electronic Submission Template for Medical Device 510 (k) Submissions...

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

https://www.fda.gov/medical-devices/premarket-notification-510k/content-510k

WebFor any device, the 510 (k) is formatted essentially the same way and contains the same basic information (required elements). This section is a general guide for all 510 (k)'s. Please...

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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...

DA: 82 PA: 76 MOZ Rank: 95