Sparco, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sparco, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Sparco, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1984 to 1988. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sparco, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sparco, Inc.
6 devices
Cleared
Oct 07, 1988
MASTER-GUARD
General Hospital
11d
Cleared
Oct 24, 1986
LIMB-GUARD
General & Plastic Surgery
14d
Cleared
Apr 15, 1985
SPARCO SCOPE GUARD
General Hospital
82d
Cleared
Feb 27, 1985
SPARCO PIGGY-BACK POLE-INTRAVENOUS TRANSPORT POLE
General & Plastic Surgery
35d
Cleared
Nov 19, 1984
FLASH GUARD PLASTIC VERSION
General & Plastic Surgery
14d
Cleared
Jun 05, 1984
FLASH GUARD
General & Plastic Surgery
43d