ClearanceBrief
Company ยท US

Reverse Medical Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2015. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DQYCatheter, Percutaneous5
KRDDevice, Vascular, For Promoting Embolization4
MMXDevice, Percutaneous Retrieval1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 22, 2015K150108Reverse Medical Micro Vascular Plug System
Reverse Medical Corporation
KRD
Jun 18, 2014K141313REVERSE MEDICAL MICRO VASCULAR PLUG SYSTEM
Reverse Medical Corporation
KRD
Nov 27, 2013K133282REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
Reverse Medical Corporation
KRD
Oct 11, 2013K130858REVERSE MEDICAL MICROCATHETER
Reverse Medical Corporation
DQY
Jul 2, 2013K123803REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM
Reverse Medical Corporation
KRD
Dec 7, 2012K122684REVERSE MEDICAL MICROCATHETER
Reverse Medical Corporation
DQY
Nov 2, 2011K112262REFLEX BALLON GUIDE CATHETER
Reverse Medical Corporation
DQY
Apr 15, 2011K102418REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM
Reverse Medical Corporation
DQY
Apr 5, 2011K110055REVERSE MEDICAL REFLEX GUIDE CATHETER
Reverse Medical Corporation
DQY
Jul 30, 2009K091563RECRUIT MICROCATHETER
Reverse Medical Corporation
MMX

Latest recalls

DateFirm and productCodeLinked 510(k)
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