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Catheter, Peritoneal Dialysis, Single Use

FDA product code FKO · 16 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
1976-10-20 – 1998-06-26
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