EMD
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Hemostat, Surgical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.4565
- Medical specialty
- Dental
- Adverse events (MAUDE)
- 1992: 1 · 2002: 1
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 |
|---|---|---|
| HEMOSTAT, SURGICAL (VARIOUS TYPES) (K920883) | S.T.S Instruments | 1992-03-13 |
| HEMOSTAT (K770158) | Deringer-Ney, Inc. | 1977-01-31 |
Track EMD automatically
Every clearance here is in the API, with alerts when new ones post.