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System, Dialysate Delivery, Semi-Automatic, Peritoneal

FDA product code KPF · 13 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.5630
Review panel
GU
Implant
No
Life sustaining
Yes
Third party review
No
GMP exempt
No
Clearance span
1979-02-16 – 2006-09-11
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