American Surgical Instruments Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Surgical Instruments Corp. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
American Surgical Instruments Corp. has 5 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 5 cleared submissions from 1990 to 1993. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by American Surgical Instruments Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Surgical Instruments Corp.
6 devices
Cleared
Nov 08, 1993
DISPOSABLE UNIPOLAR COAGULATOR PROBE SYSTEM
Obstetrics & Gynecology
578d
Cleared
May 13, 1993
IRRIGATION PUMPS AND TUBING AND SUCTION TUBING
General & Plastic Surgery
413d
Cleared
Mar 09, 1992
NEZHAT/DORSEY HYDRO DISSECTION PUMP & ACCESSORIES
Obstetrics & Gynecology
187d
Cleared
Nov 01, 1991
NEZHAT DORSEY SUCTION PROBE W/INNER IRRIGA TUBE
General & Plastic Surgery
56d
Cleared
Jun 20, 1991
UNIPOLAR COAGULATOR PROBE SYSTEM
General & Plastic Surgery
90d
Cleared
Mar 28, 1990
NEZHAT/DORSEY HYDRO DISSECTION PUMP OB-GYN USE
Obstetrics & Gynecology
156d