American Lasers, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Lasers, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
American Lasers, Inc. has 5 FDA 510(k) cleared medical devices. Based in Alhambra, US.
Historical record: 5 cleared submissions from 1995 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Lasers, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Lasers, Inc.
5 devices
Cleared
Sep 29, 2006
MINI-YAG LASER
General & Plastic Surgery
91d
Cleared
Jan 28, 1998
HM-RUBY
General & Plastic Surgery
86d
Cleared
Sep 29, 1997
MM-RUBY
General & Plastic Surgery
234d
Cleared
Nov 29, 1995
AM RUBY
General & Plastic Surgery
279d
Cleared
Aug 28, 1995
AM-YAG
General & Plastic Surgery
186d