Hgm Medical Laser Systems, Inc.
Hgm Medical Laser Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1992.
Top product codes for Hgm Medical Laser Systems, Inc.
Recent clearances by Hgm Medical Laser Systems, Inc.
- K921300 — MODEL PC ARGON ION LASER
- K914484 — LITESPOT(TM) LASER INDIRECT OPHTHALMOSCOPE
- K913569 — COMPAC A, ELITE A, ELITE A PLUS, SURGICA A
- K912628 — AIR ARGON ION LASERS VARIOUS MODELS
- K910272 — HGM COMBINATION ND:YAG & SOLID STATE GREEN
- K912438 — MODELS 5,8,20,20S ARGON ION LASERS
- K910602 — HGM ARGON ION & SOLID LIGHT LASER FOR DENTISTRY
- K911104 — PHOTCOAGULATOR KR-568 LASER SPECTRUM ELITE K1
- K910898 — SURGICA(TM) H
- K904699 — COMPAC(TM) DIODE LASERS
- K904700 — ENDOCOAGULATOR KRS568(TM) LASER
- K904342 — SERIES 1990 ARGON SURGICAL LASERS, E1,E6,E14&E20A
- K902258 — 5 MM IRRIGATION/ASPIRATION FIBER PROBE
- K896314 — ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG
- K901021 — F300 SERIES CONTACT FIBER HANDPIECES
- K881507 — ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIES
- K890787 — O-020 LASER INDIRECT OPHTHALMOSCOPE
- K881940 — MODEL 20 KY KRYPTON YELLOW LASER
Data sourced from openFDA. This site is unofficial and independent of the FDA.