Medical Device Manufacturer · US , Salt Lake City , UT

American Laser Medical - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1996

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

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
1-5 of 5
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