Premier Laser Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Premier Laser Systems, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
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