Hgm Medical Laser Systems, Inc.
Salt Lake City, UT, US
Hgm Medical Laser Systems, Inc. appears in FDA device records in Salt Lake City, UT. FDA records list 18 510(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
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Hgm Medical Laser Systems, Inc. between 1988 and 1992. The busiest year on record is 1991, with 9. The most recent is 1992, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1989 | 2 |
| 1990 | 4 |
| 1991 | 9 |
| 1992 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K921300 | MODEL PC ARGON ION LASER | GEX | Substantially Equivalent | |
| K914484 | LITESPOT(TM) LASER INDIRECT OPHTHALMOSCOPE | HLI | Substantially Equivalent | |
| K913569 | COMPAC A, ELITE A, ELITE A PLUS, SURGICA A | GEX | Substantially Equivalent | |
| K912628 | AIR ARGON ION LASERS VARIOUS MODELS | GEX | Substantially Equivalent | |
| K910272 | HGM COMBINATION ND:YAG & SOLID STATE GREEN | GEX | Substantially Equivalent | |
| K912438 | MODELS 5,8,20,20S ARGON ION LASERS | GEX | Substantially Equivalent | |
| K910602 | HGM ARGON ION & SOLID LIGHT LASER FOR DENTISTRY | GEX | Substantially Equivalent | |
| K911104 | PHOTCOAGULATOR KR-568 LASER SPECTRUM ELITE K1 | FEX | Substantially Equivalent | |
| K910898 | SURGICA(TM) H | GEX | Substantially Equivalent | |
| K904699 | COMPAC(TM) DIODE LASERS | HQF | Substantially Equivalent | |
| K904700 | ENDOCOAGULATOR KRS568(TM) LASER | GEX | Substantially Equivalent | |
| K904342 | SERIES 1990 ARGON SURGICAL LASERS, E1,E6,E14&E20A | GEX | Substantially Equivalent | |
| K902258 | 5 MM IRRIGATION/ASPIRATION FIBER PROBE | HET | Substantially Equivalent | |
| K896314 | ENDOSCOPIC USES OF THE ARGON LASER IN GENERAL SURG | GEX | Substantially Equivalent | |
| K901021 | F300 SERIES CONTACT FIBER HANDPIECES | GEX | Substantially Equivalent | |
| K881507 | ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIES | HHR | Substantially Equivalent | |
| K890787 | O-020 LASER INDIRECT OPHTHALMOSCOPE | HGF | Substantially Equivalent | |
| K881940 | MODEL 20 KY KRYPTON YELLOW LASER | GEX | 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