American Laser Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Laser Medical - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
American Laser Medical has 5 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 5 cleared submissions from 1996 to 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Laser Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Laser Medical
5 devices
Cleared
Mar 22, 1999
NUVOLASE 532 CUTANEOUS LASER SYSTEM
General & Plastic Surgery
13d
Cleared
Oct 21, 1997
NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASER
General & Plastic Surgery
89d
Cleared
Oct 06, 1997
NUVOLASE 660 LASER SYSTEM FOR OPHTHALMOLOGY
General & Plastic Surgery
89d
Cleared
May 13, 1997
NUVO-LASE 660 LASER SYSTEM
General & Plastic Surgery
78d
Cleared
Nov 26, 1996
FLEX-LASE 600 SERIES ION LASER SYSTEM
General & Plastic Surgery
90d