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Catheter, Double Lumen Female Urethrographic

FDA product code FGH · 1 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
1991-03-27 – 1991-03-27
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