A-Med Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
A-Med Systems, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
A-Med Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in West Sacramento, US.
Historical record: 4 cleared submissions from 1999 to 2002. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by A-Med Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - A-Med Systems, Inc.
4 devices
Cleared
Aug 26, 2002
LARGE CENTRIFUGAL BLOOD PUMP, MODEL CP-2
Cardiovascular
188d
Cleared
Nov 09, 2001
HEPARIN COATED MINIATURE CENTRIFUGAL BYPASS PUMP SYSTEM
Cardiovascular
25d
Cleared
May 04, 2000
A-MINIATURE CENTRIFUGAL BLOOD PUMP SYSTEM, MODEL CPB 2000
Cardiovascular
276d
Cleared
Dec 28, 1999
A-MED VASCULAR CANNULA, MODELS V24-10-08, V24-10-16, V24-10-32, V24-21-08,...
Cardiovascular
239d