Sparta Surgical Corp. - FDA 510(k) Cleared Devices
7
Total
6
Cleared
0
Denied
Sparta Surgical Corp. has 6 FDA 510(k) cleared medical devices. Based in Hayward, US.
Historical record: 6 cleared submissions from 1989 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sparta Surgical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Sparta Surgical Corp.
7 devices
Cleared
Aug 01, 1997
SPECTRUM II, SPECTRUM PLUS, AND SPECTRUM MAX-SD
Neurology
220d
Cleared
Jan 12, 1995
SPARTA HYDROGEL WOUND DRESSING
General & Plastic Surgery
72d
Cleared
Nov 23, 1992
SPARTA WET DRESSING, SODIUM CHLORIDE
General & Plastic Surgery
171d
Cleared
Mar 22, 1991
DAVID SIMMONDS ANESTHESIA EXTENSION TUBES
General Hospital
113d
Cleared
Feb 06, 1991
VESSELOOPS
General & Plastic Surgery
78d
Cleared
Nov 08, 1989
SURGI-BRUSH
General & Plastic Surgery
20d
Cleared
Nov 02, 1989
MICROSPEARS
Ophthalmic
14d