Premier Laser Systems, Inc. is one of 8144 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Premier Laser Systems, Inc. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Irvine, US.
Historical record: 14 cleared submissions from 1994 to 1999.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Premier Laser Systems, Inc.
14 devices
Cleared
Nov 18, 1999
AURORA SL
General & Plastic Surgery
49d
Cleared
Sep 22, 1999
AURORA HL
General & Plastic Surgery
69d
Cleared
Aug 20, 1999
BLULAZE
General & Plastic Surgery
15d
Cleared
Nov 23, 1998
AURORA
General & Plastic Surgery
221d
Cleared
Oct 09, 1998
CENTAURI
General & Plastic Surgery
25d
Cleared
Aug 24, 1998
PEGASUS ND:YAG LASER SYSTEM
General & Plastic Surgery
192d
Cleared
Jul 15, 1998
AURORA DIODE LASER SYSTEM
General & Plastic Surgery
218d
Cleared
Mar 19, 1998
DERMIUM
General & Plastic Surgery
34d
Cleared
Dec 16, 1997
ARAGO
General & Plastic Surgery
270d
Cleared
May 05, 1997
CENTAURI
General & Plastic Surgery
1432d
Cleared
May 05, 1997
CENTAURI
General & Plastic Surgery
1370d
Cleared
Aug 15, 1996
ARGON CURING LASER
General & Plastic Surgery
106d
Cleared
Dec 15, 1995
AURORA SURGICAL DIODE LASER SYSTEM W/ACCESSORIES
General & Plastic Surgery
91d
Cleared
Mar 14, 1994
PEGASUS
General & Plastic Surgery
516d