Hgm, Inc.
Hgm, Inc. appears in FDA public data with 0 recalls, 23 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 11, 1995.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 23
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K950120 | SMART PLUG | August 11, 1995 |
| K931072 | HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE | November 10, 1994 |
| K931784 | HGM ILLUMINATING IMAGING ENDOCULAR PROBE | March 1, 1994 |
| K933333 | HGM SCANMAN PLUS | September 23, 1993 |
| K931499 | Q-11 OPHTHALMIC LASER | August 19, 1993 |
| K925663 | HGM ASPIRATING ENDOOCULAR(TM) PROBE | August 17, 1993 |
| K930543 | E-25 KRYPTON ION LASER (SURGICA K5) | June 22, 1993 |
| K880908 | MODEL PC ARGON LASER | May 3, 1988 |
| K873773 | ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER | October 13, 1987 |
| K872630 | ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO. | August 25, 1987 |
| K870773 | ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER | July 10, 1987 |
| K871424 | ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER | July 8, 1987 |
| K862227 | MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN | August 19, 1986 |
| K860357 | HGM, INC. LASERCATH (STERILE) | April 7, 1986 |
| K860358 | FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE (STERILE) | March 21, 1986 |
| K852913 | HGM ENDOCOAGULATOR MODEL 20 | September 5, 1985 |
| K851651 | HGM ENDOCOAGULATOR MODEL 8 | July 23, 1985 |
| K850572 | HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K | April 23, 1985 |
| K840590 | FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE | May 9, 1984 |
| K840854 | MEDICAL LASER ENDOCOAGULATOR 5K | April 2, 1984 |