Keyword Analysis & Research: fda 510k clearance lookup


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Keyword CPC PCC Volume Score Length of keyword
fda 510k clearance lookup0.940.698775025
fda1.660.39286473
510k0.170.59796694
clearance0.531203919
lookup1.010.84515436

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Keyword CPC PCC Volume Score
fda 510k clearance lookup0.680.6527185

Search Results related to fda 510k clearance lookup on Search Engine

  • 510(k) Clearances | FDA

    fda.gov

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

    Aug 31, 2021 · 510 (k) Clearances Overview Section 510 (k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA of their intent to market a …

    DA: 57 PA: 71 MOZ Rank: 24

  • Search the Releasable 510(k) Database | FDA

    fda.gov

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

    You 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: 64 PA: 13 MOZ Rank: 23

  • May 2021 510(K) Clearances | FDA

    fda.gov

    https://www.fda.gov/medical-devices/510k-clearances/may-2021-510k-clearances

    Jun 08, 2021 · 510 (K) SUMMARIES OR 510 (K) STATEMENTS FOR FINAL DECISIONS RENDERED DURING THE PERIOD May 2021 DEVICE: Neuro-IOM system with Neuro …

    DA: 95 PA: 55 MOZ Rank: 83

  • 510(k) Devices Cleared in 2021 | FDA

    fda.gov

    https://www.fda.gov/medical-devices/510k-clearances/510k-devices-cleared-2021

    Jan 04, 2022 · March 2021 510 (K) Clearances. April 2021 510 (K) Clearances. May 2021 510 (K) Clearances. June 2021 510 (K) Clearances. July 2021 510 (K) Clearances. August 2021 …

    DA: 18 PA: 65 MOZ Rank: 54

  • February 2021 510(K) Clearances | FDA

    fda.gov

    https://www.fda.gov/medical-devices/510k-clearances/february-2021-510k-clearances

    Mar 06, 2021 · 510 (K) SUMMARIES OR 510 (K) STATEMENTS FOR FINAL DECISIONS RENDERED DURING THE PERIOD February 2021 DEVICE: Archworx Utah Medical …

    DA: 33 PA: 10 MOZ Rank: 91

  • Device Approvals, Denials and Clearances | FDA

    fda.gov

    https://www.fda.gov/medical-devices/products-and-medical-procedures/device-approvals-denials-and-clearances

    a 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 …

    DA: 84 PA: 83 MOZ Rank: 49

  • 510(k) Premarket Notification - Food and Drug …

    fda.gov

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

    FDA Home 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 …

    DA: 62 PA: 35 MOZ Rank: 70

  • 510(K) Premarket Notification - Food and Drug …

    fda.gov

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

    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...

    DA: 70 PA: 61 MOZ Rank: 13

  • 510(k) Clearances - Food and Drug Administration

    fda.gov

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

    510 (k) Clearances A 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...

    DA: 27 PA: 7 MOZ Rank: 12

  • 510(K) Premarket Notification - Food and Drug …

    fda.gov

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

    DIAGNOSTIC PRODUCTS CORP. k000257. 02/23/2000. screeners cocaine test; drugscreen dip cocaine test. DRUG DETECTION DEVICES, LTD. k000350. 04/11/2000. mityview 4-way … clearance lookup

    clearance lookup

    DA: 99 PA: 46 MOZ Rank: 33