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Container, Transport, Kidney

FDA product code KDK · 3 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.5880
Review panel
GU
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1980-09-26 – 2006-01-17
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