Medical Device Manufacturer · US , Salt Lake City , UT

Hgm, Inc. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 1983

23

Total

23

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hgm, Inc. Gastroenterology & Urology ✕

3 devices

1-3 of 3

Cleared Aug 25, 1987

ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO.

Gastroenterology & Urology · 50d

Cleared Apr 07, 1986

HGM, INC. LASERCATH (STERILE)

Gastroenterology & Urology · 67d

Cleared Sep 05, 1985

HGM ENDOCOAGULATOR MODEL 20

Gastroenterology & Urology · 56d