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Endoscope, Fiber Optic

FDA product code GDB · 7 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.1500
Review panel
GU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1981-01-15 – 2003-08-20
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