HFL
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Drain, Cervical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.3200
- Medical specialty
- Obstetrics/Gynecology
- Adverse events (MAUDE)
- 1993: 1 · 1995: 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 |
|---|---|---|
| SIL-MED T-TUBE DRAIN (K903989) | Sil-Med Corp. | 1991-01-31 |
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Every clearance here is in the API, with alerts when new ones post.