HGF
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Source, Abortion Unit, Vacuum
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.5070
- Medical specialty
- Obstetrics/Gynecology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| BOTTLE COLLECTION SET (K945179) | Medgyn Products, Inc. | 1995-01-26 |
| BIOVISION ENDOCULAR PROBE (K905115) | Douglas James Donaldson Compliance Services | 1991-02-11 |
| MODEL GLASE 210 HOLMIUM LASER SYSTEM (K904248) | Charles L. Rose and Co., Inc. | 1990-12-14 |
| O-020 LASER INDIRECT OPHTHALMOSCOPE (K890787) | Hgm Medical Laser Systems, Inc. | 1989-03-24 |
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Every clearance here is in the API, with alerts when new ones post.