Reverse Medical Corporation is one of 18459 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reverse Medical Corporation - FDA 510(k) Cleared Devices
Recent clearances: Reverse Medical Micro Vascular Plug System, REVERSE MEDICAL MICRO VASCULAR PLUG SYSTEM, REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
10
Total
10
Cleared
0
Denied
Reverse Medical Corporation has 10 FDA 510(k) cleared cardiovascular devices. Based in Irvine, US.
Historical record: 10 cleared submissions from 2009 to 2015.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Reverse Medical Corporation
10 devices
Cleared
Apr 22, 2015
Reverse Medical Micro Vascular Plug System
Cardiovascular
92d
Cleared
Jun 18, 2014
REVERSE MEDICAL MICRO VASCULAR PLUG SYSTEM
Cardiovascular
29d
Cleared
Nov 27, 2013
REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
Cardiovascular
33d
Cleared
Oct 11, 2013
REVERSE MEDICAL MICROCATHETER
Cardiovascular
197d
Cleared
Jul 02, 2013
REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
Cardiovascular
204d
Cleared
Dec 07, 2012
REVERSE MEDICAL MICROCATHETER
Cardiovascular
98d
Cleared
Nov 02, 2011
REFLEX BALLON GUIDE CATHETER
Cardiovascular
86d
Cleared
Apr 15, 2011
REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM
Cardiovascular
233d
Cleared
Apr 05, 2011
REVERSE MEDICAL REFLEX GUIDE CATHETER
Cardiovascular
85d
Cleared
Jul 30, 2009
RECRUIT MICROCATHETER
Cardiovascular
63d