Search Results related to fda 510k database on Search Engine
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Search the Releasable 510(k) Database | FDA
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 …
DA: 28 PA: 30 MOZ Rank: 72
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510(k) Premarket Notification - Food and Drug Administration
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm
WebApr 15, 2024 · FDA Home. Medical Devices. Databases. A 510 (K) is a premarket submission made to FDA to demonstrate that the device to be …
DA: 29 PA: 30 MOZ Rank: 86
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510(k) Clearances | FDA - U.S. Food and Drug Administration
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) …
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510(k) Clearances | FDA - U.S. Food and Drug Administration
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; …
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510(K) Premarket Notification - Food and Drug Administration
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 …
DA: 45 PA: 44 MOZ Rank: 56