Adapta Medical, Inc. is one of 16094 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Adapta Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PerfIC Cath Gel S, PerfIC Cath Gel C, PerfIC Cath Hydro S, PerfIC Cath Hydro C, COLORADO CATHETER STERILESURE - NEW NAME PERFIC CATH
2
Total
2
Cleared
0
Denied
Adapta Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Denver, US.
Historical record: 2 cleared submissions from 2011 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Adapta Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Neil Burris & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Adapta Medical, Inc.
2 devices