American Laser Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
American Laser Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1982 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Laser Corp. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Apr 05, 2001
NUVOLASE 532 MEDICAL LASER SYSTEM
General & Plastic Surgery
90d
Cleared
May 17, 1999
BQ/BM INTEGRATED LASER DELIVERY SYSTEM
Ophthalmic
76d
Cleared
Mar 22, 1999
NUVOLASE 532 LASER SYSTEM
General & Plastic Surgery
17d
Cleared
Jan 07, 1983
LASER PHOTOCOAGULATOR
Radiology
80d
Cleared
Jan 22, 1982
LASER PHOTOCOAGULATOR ARGON MED. LASER
Hematology
45d