FML
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Chair, Blood Donor
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6140
- Medical specialty
- General Hospital
- Flags
- GMP exempt
- Adverse events (MAUDE)
- 1993: 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 |
|---|---|---|
| UNILET LANCET (K842517) | Ulster Scientific, Inc. | 1984-09-20 |
| GLOVES, FLOOR (K780181) | Tillotson Rubber Co., Inc. | 1978-02-21 |
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Every clearance here is in the API, with alerts when new ones post.