MAB
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Marker, Cardiopulmonary Bypass (Vein Marker)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.3450
- Medical specialty
- Cardiovascular
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SUTURING WASHER (K052642) | First Call, Inc. | 2006-01-17 |
| GRAFT MARKER RING (K001915) | T. Korossurgical Instruments Corp. | 2001-04-27 |
| C.A.B. RING (K894268) | Medi-Sharp, Inc. | 1989-08-17 |
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Every clearance here is in the API, with alerts when new ones post.