Possis Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Possis Medical, Inc. - FDA 510(k) Cleared Devices
34
Total
34
Cleared
0
Denied
Possis Medical, Inc. has 34 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 34 cleared submissions from 1983 to 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Possis Medical, Inc.
34 devices
Cleared
Feb 14, 2014
ANGIOJET ULTRA AVX THROMBECTOMY SET
Cardiovascular
80d
Cleared
Jun 22, 2009
ANGIO JET ULTRA DVX AND XPEEDIOR THROMBECTOMY SETS
Cardiovascular
20d
Cleared
Apr 08, 2009
ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL 106552-001, ANGIOJET ULTRA...
Cardiovascular
65d
Cleared
Dec 12, 2008
ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039
Cardiovascular
115d
Cleared
Sep 26, 2008
MODIFICATION TO FETCH ASPIRATION CATHETER
Cardiovascular
74d
Cleared
Jun 13, 2008
GUARDDOG OCCLUSION GUIDEWIRE, INFLATION DEVICE
Cardiovascular
21d
Cleared
Apr 04, 2008
ANGIOJET ULTRA SPIROFLEX VG THROMBECTOMY SET, MODEL 106608
Cardiovascular
14d
Cleared
Jan 24, 2008
ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039
Cardiovascular
48d
Cleared
Nov 14, 2007
ANGIOJET ULTRA
Cardiovascular
47d
Cleared
Sep 08, 2007
ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL: 106552
Cardiovascular
24d
Cleared
Aug 24, 2007
ANGIOJET XPEEDIOR RHEOLYTIC THROMBECTOMY CATHETER, MODEL 104307
Cardiovascular
105d
Cleared
Jul 31, 2007
ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040, 105042, 106552,...
Cardiovascular
78d