Angeion Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Angeion Corp. Cardiovascular ✕
5 devices
Cleared
Mar 18, 1993
ANGEION IGITAL ANGEFLATOR
Cardiovascular
339d
Cleared
Dec 13, 1990
ANGEFLATOR(TM)
Cardiovascular
197d
Cleared
Apr 30, 1990
Y-ADAPTER W/THOUY BORST
Cardiovascular
227d
Cleared
Nov 30, 1989
ANGEION HEMOSTASIS VALVE INTRODUCER
Cardiovascular
136d
Cleared
Jun 24, 1987
CATHETER INTRODUCER
Cardiovascular
92d