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Light, Catheter, Fiberoptic, Glass, Ureteral

FDA product code FCS · 9 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.4020
Review panel
GU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1988-03-22 – 2006-09-28
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