Avecor Cardiovascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avecor Cardiovascular, Inc. - FDA 510(k) Cleared Devices
9
Total
8
Cleared
0
Denied
Avecor Cardiovascular, Inc. has 8 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 8 cleared submissions from 1993 to 1998. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Avecor Cardiovascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avecor Cardiovascular, Inc.
9 devices
Cleared
Feb 18, 1998
AFFINITY HOLLOW FIBER OXYGENATOR WITH TRILLIUM BIOPASSIVE SURFACE
Cardiovascular
139d
Cleared
Aug 05, 1997
AFFINITY BLOOD PUMP SYSTEM
Cardiovascular
302d
Cleared
Jul 11, 1997
MYOTHERM (TM) XP CARDIOPLEGIA DELIVERY SYSTEM
Cardiovascular
107d
Cleared
Oct 06, 1995
AFFINITY ARTERIAL BLOOD FILTER
Cardiovascular
127d
Cleared
Jun 28, 1994
AVECOR PRE-BYPASS FILTER
Cardiovascular
169d
Cleared
Jun 20, 1994
AFFINITY CVR
Cardiovascular
186d
Cleared
May 10, 1994
AFFINITY VENOUS RESERVIOR BAG
Cardiovascular
161d
Cleared
Nov 19, 1993
AFFINITY HOLLOW FIBER OXYGENATOR
Cardiovascular
177d
Cleared
Jun 23, 1993
SIGNATURE(TM) CUSTOM TUBING PACK
Cardiovascular
288d