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Tubing, Pump, Cardiopulmonary Bypass

FDA product code DWE · 19 cleared devices

Class 2 Cardiovascular
Regulation
21 CFR 870.4390
Review panel
CV
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1980-02-21 – 2024-08-08
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