Hgm, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
23
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K950120SMART PLUGAugust 11, 1995
K931072HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBENovember 10, 1994
K931784HGM ILLUMINATING IMAGING ENDOCULAR PROBEMarch 1, 1994
K933333HGM SCANMAN PLUSSeptember 23, 1993
K931499Q-11 OPHTHALMIC LASERAugust 19, 1993
K925663HGM ASPIRATING ENDOOCULAR(TM) PROBEAugust 17, 1993
K930543E-25 KRYPTON ION LASER (SURGICA K5)June 22, 1993
K880908MODEL PC ARGON LASERMay 3, 1988
K873773ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASEROctober 13, 1987
K872630ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO.August 25, 1987
K870773ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASERJuly 10, 1987
K871424ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASERJuly 8, 1987
K862227MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYNAugust 19, 1986
K860357HGM, INC. LASERCATH (STERILE)April 7, 1986
K860358FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE (STERILE)March 21, 1986
K852913HGM ENDOCOAGULATOR MODEL 20September 5, 1985
K851651HGM ENDOCOAGULATOR MODEL 8July 23, 1985
K850572HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-KApril 23, 1985
K840590FLEISCHMAN-SWARTZ ENDO-OCULAR PROBEMay 9, 1984
K840854MEDICAL LASER ENDOCOAGULATOR 5KApril 2, 1984