Hgm, Inc.
Hgm, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1995.
Top product codes for Hgm, Inc.
Recent clearances by Hgm, Inc.
- K950120 — SMART PLUG
- K931072 — HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE
- K931784 — HGM ILLUMINATING IMAGING ENDOCULAR PROBE
- K933333 — HGM SCANMAN PLUS
- K931499 — Q-11 OPHTHALMIC LASER
- K925663 — HGM ASPIRATING ENDOOCULAR(TM) PROBE
- K930543 — E-25 KRYPTON ION LASER (SURGICA K5)
- K880908 — MODEL PC ARGON LASER
- K873773 — ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER
- K872630 — ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO.
- K870773 — ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER
- K871424 — ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER
- K862227 — MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN
- K860357 — HGM, INC. LASERCATH (STERILE)
- K860358 — FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE (STERILE)
- K852913 — HGM ENDOCOAGULATOR MODEL 20
- K851651 — HGM ENDOCOAGULATOR MODEL 8
- K850572 — HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K
- K840590 — FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE
- K840854 — MEDICAL LASER ENDOCOAGULATOR 5K
- K837422 — LASER PHOTOCOAGULATOR
- K837306 — LASER PHOTOCOAGULATOR
- K827847 — ARGON FIBER OPTIC CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.