Infusaid Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Infusaid Corp. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Infusaid Corp. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 8 cleared submissions from 1983 to 1991. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Infusaid Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Infusaid Corp.
8 devices
Cleared
Nov 21, 1991
SNAP-LOCK MICRO PORT, MODIFICATION
General Hospital
303d
Cleared
Sep 05, 1990
DUAL PORT
General Hospital
163d
Cleared
Jul 31, 1990
SUBCLAVIAN INTRODUCER SET
Cardiovascular
76d
Cleared
Apr 29, 1986
SUBCLAVIAN INTRODUCER SET
Cardiovascular
50d
Cleared
Sep 18, 1984
INFUSE-A-PORT HEPARIN LOCK MAINT KIT
General Hospital
225d
Cleared
Aug 06, 1984
INFUSAID INFUSE-A-PORT
General Hospital
46d
Cleared
Sep 15, 1983
INFUSE-A-PORT
General Hospital
27d
Cleared
Jan 12, 1983
INFUSE-A-PORT
General Hospital
15d