HHF
6 FDA 510(k) clearances · Product code
91 daysmedian time to decision
421 days90th percentile
6clearances measured
FDA profile
- Official device name
- Remover, Intrauterine Device, Contraceptive, Hook-Type
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 884.4530
- Medical specialty
- Obstetrics/Gynecology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| IUD HOOKS (K926541) | Thomasville Medical Assoc. | 1994-02-24 |
| IUD HOOKS - SIMPLE, UNIVERSAL AND SKLAR (K891030) | Zinnanti Surgical Instruments, Inc. | 1989-03-17 |
| INTRAUTERINE DEVICE REMOVER (K842295) | Premier Dental Products Co. | 1984-10-12 |
| RELIANCE TEMPO OPHTH. INSTR STAND (K831568) | F. & F. Koenigkramer | 1983-06-30 |
| EMMETT IUD THREAD RETREIVER (K820115) | Proto-Med, Inc. | 1982-02-05 |
| THE EMMETT IUD THREAD RETRIEVER (K811761) | Proto-Med, Inc. | 1981-09-21 |
Track HHF automatically
Every clearance here is in the API, with alerts when new ones post.