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Catheter, Urethrographic, Male

FDA product code FGI · 3 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.5130
Review panel
GU
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1981-03-20 – 2002-12-10
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