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Catheter, Rectal For Continent Ileostomy

FDA product code KPH · 1 cleared devices

Class 1 Gastroenterology, Urology
Regulation
21 CFR 876.5030
Review panel
GU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1981-12-31 – 1981-12-31
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