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Dilator, Vessel

FDA product code FKA · 3 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.5540
Review panel
GU
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1991-04-29 – 2002-10-11
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