Hgm, Inc.
Salt Lake City, UT, US
Hgm, Inc. appears in FDA device records in Salt Lake City, UT. FDA records list 21 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Hgm, Inc. between 1983 and 1995. The busiest year on record is 1987, with 4. The most recent is 1995, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 3 |
| 1985 | 3 |
| 1986 | 3 |
| 1987 | 4 |
| 1988 | 1 |
| 1993 | 4 |
| 1994 | 2 |
| 1995 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K950120 | SMART PLUG | GEX | Substantially Equivalent | |
| K931072 | HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE | HJM | Substantially Equivalent | |
| K931784 | HGM ILLUMINATING IMAGING ENDOCULAR PROBE | HQF | Substantially Equivalent | |
| K933333 | HGM SCANMAN PLUS | GEX | Substantially Equivalent | |
| K931499 | Q-11 OPHTHALMIC LASER | GEX | Substantially Equivalent | |
| K925663 | HGM ASPIRATING ENDOOCULAR(TM) PROBE | HQF | Substantially Equivalent | |
| K930543 | E-25 KRYPTON ION LASER (SURGICA K5) | GEX | Substantially Equivalent | |
| K880908 | MODEL PC ARGON LASER | GEX | Substantially Equivalent | |
| K873773 | ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER | GEX | Substantially Equivalent | |
| K872630 | ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO. | LNK | Substantially Equivalent | |
| K870773 | ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER | LLF | Substantially Equivalent | |
| K871424 | ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER | LMS | Substantially Equivalent | |
| K862227 | MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN | HHR | Substantially Equivalent | |
| K860357 | HGM, INC. LASERCATH (STERILE) | LNK | Substantially Equivalent | |
| K860358 | FLEISCHMAN-SWARTZ ENDO-OCULAR PROBE (STERILE) | HQF | Substantially Equivalent | |
| K852913 | HGM ENDOCOAGULATOR MODEL 20 | Substantially Equivalent | ||
| K851651 | HGM ENDOCOAGULATOR MODEL 8 | Substantially Equivalent | ||
| K850572 | HGM, INC. MEDICAL LASER ENDOCOAGULATOR MODEL 8-K | HQF | Substantially Equivalent | |
| K837422 | LASER PHOTOCOAGULATOR | Substantially Equivalent | ||
| K837306 | LASER PHOTOCOAGULATOR | Substantially Equivalent | ||
| K827847 | ARGON FIBER OPTIC CATHETER | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain