American Laser Medical - FDA 510(k) Cleared Devices
Recent clearances: NUVOLASE 532 CUTANEOUS LASER SYSTEM, NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASER, NUVOLASE 660 LASER SYSTEM FOR OPHTHALMOLOGY
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - American Laser Medical General & Plastic Surgery ✕
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