MAB
2006-01-17
Marker, Cardiopulmonary Bypass (Vein Marker)
FDA product code MAB · 3 cleared devices
Class 2
Cardiovascular
- Regulation
- 21 CFR 870.3450
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1989-08-17 – 2006-01-17
No matching devices.
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