Angeion Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Angeion Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Angeion Corp. has 7 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 7 cleared submissions from 1987 to 1993. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Angeion Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Angeion Corp.
7 devices
Cleared
Mar 18, 1993
ANGEION IGITAL ANGEFLATOR
Cardiovascular
339d
Cleared
Jan 12, 1993
ANGESTAT(R) PERICARDIAL DRAINAGE SHEATH SET
General & Plastic Surgery
71d
Cleared
Feb 18, 1992
ANGEION ENDOSCOPIC VALVE SEAL
Gastroenterology & Urology
60d
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