The Food and Drug Administration's (FDA's) 510(k) Process: A Systematic Review of 1000 Cases

Author:

Shah Puja,Olavarria Oscar,Dhanani Naila,Ciomperlik Hailie,Mohr Cassandra,Bernardi Karla,Neela Niharika,Coelho Rainna,Ali ZuhairORCID,Prabhu Ajita,Liang Mike K.

Publisher

Elsevier BV

Subject

General Medicine

Reference79 articles.

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2. EMERGO by UL. USA – Overview of medical device industry and healthcare statistics. Available at: https://www.emergobyul.com/resources/market-united-states. Accessed October 20, 2020.

3. Drug Watch. FDA 510(k) clearance process. Available at: https://www.drugwatch.com/fda/510k-clearance/. Accessed October 20, 2020.

4. LaVito A. CNBC. FDA to overhaul more than 40-year-old process for approving medical devices that some say puts consumers at risk. Available at: https://www.cnbc.com/2018/11/26/fda-to-overhaul-510k-medical-device-approval-process.html. Accessed October 20, 2020.

5. U.S. Food & Drug Administration. CFR - Code of Federal Regulations Title 21. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?fr=807.92. Accessed October 20, 2020.

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