HGC
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Clamp, Uterine
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 884.4520
- Medical specialty
- Obstetrics/Gynecology
- Adverse events (MAUDE)
- 1992: 1 · 2005: 5 · 2006: 2
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| UTERINE CLAMPS (K891402) | Zinnanti Surgical Instruments, Inc. | 1989-03-29 |
| GUSBERG HYSTERECTOMY CLAMP (K771344) | J. Sklar Mfg. Co., Inc. | 1977-07-27 |
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Every clearance here is in the API, with alerts when new ones post.