American Surgical Laser, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Surgical Laser, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
American Surgical Laser, Inc. has 5 FDA 510(k) cleared medical devices. Based in Woburn, US.
Historical record: 5 cleared submissions from 1984 to 1985. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Surgical Laser, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Surgical Laser, Inc.
5 devices
Cleared
Feb 04, 1985
MINUTEMAN CO2 MICROSURGICAL LASER GYN
Obstetrics & Gynecology
152d
Cleared
Dec 07, 1984
MINUTEMAN CO2 MICROSURG LASER DERMATOL-
General & Plastic Surgery
93d
Cleared
Dec 07, 1984
MINUTEMAN C02 MICROSURG LASER PODIATRY
General & Plastic Surgery
93d
Cleared
Dec 07, 1984
MINUTEMAN CO2 MICROSURG LASER GEN SURG
General & Plastic Surgery
93d
Cleared
Dec 04, 1984
MINUTEMAN CO2 MICROSURGICAL LASER OTO
Ear, Nose, Throat
90d