HFD
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Washer, Endometrial
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.1185
- 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 |
|---|---|---|
| WEIGHTED SPECULA-STEINER,HENROTIN,BERLAND,GARRIGUE (K891037) | Zinnanti Surgical Instruments, Inc. | 1989-03-17 |
| VAGINAL SPECULUM (K890376) | Kinetic Medical Products | 1989-02-27 |
| SKIN SCRUB TRAY (K810558) | Associated Medical Products Co. | 1981-03-17 |
Track HFD automatically
Every clearance here is in the API, with alerts when new ones post.