EYX
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Drape, Pure Latex Sheet, With Self-Retaining Finger Cot
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4370
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DRAPE, TRANSURETHRAL RESECTION (TUR) (K760175) | V. Mueller O.V. Baxter Healthcare Corp. | 1976-08-30 |
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Every clearance here is in the API, with alerts when new ones post.