Hgm Medical Laser Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hgm Medical Laser Systems, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Hgm Medical Laser Systems, Inc. has 18 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 18 cleared submissions from 1988 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hgm Medical Laser Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hgm Medical Laser Systems, Inc.
18 devices
Cleared
Oct 06, 1992
MODEL PC ARGON ION LASER
General & Plastic Surgery
202d
Cleared
Jan 06, 1992
LITESPOT(TM) LASER INDIRECT OPHTHALMOSCOPE
Ophthalmic
90d
Cleared
Oct 17, 1991
COMPAC A, ELITE A, ELITE A PLUS, SURGICA A
General & Plastic Surgery
69d
Cleared
Sep 13, 1991
AIR ARGON ION LASERS VARIOUS MODELS
General & Plastic Surgery
88d
Cleared
Aug 09, 1991
HGM COMBINATION ND:YAG & SOLID STATE GREEN
General & Plastic Surgery
198d
Cleared
Jul 17, 1991
MODELS 5,8,20,20S ARGON ION LASERS
General & Plastic Surgery
44d
Cleared
Jun 24, 1991
HGM ARGON ION & SOLID LIGHT LASER FOR DENTISTRY
General & Plastic Surgery
131d
Cleared
Jun 11, 1991
PHOTCOAGULATOR KR-568 LASER SPECTRUM ELITE K1
Gastroenterology & Urology
90d
Cleared
May 31, 1991
SURGICA(TM) H
General & Plastic Surgery
88d
Cleared
Apr 25, 1991
COMPAC(TM) DIODE LASERS
Ophthalmic
191d
Cleared
Feb 19, 1991
ENDOCOAGULATOR KRS568(TM) LASER
General & Plastic Surgery
126d
Cleared
Dec 19, 1990
SERIES 1990 ARGON SURGICAL LASERS, E1,E6,E14&E20A
General & Plastic Surgery
89d