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Dilator, Urethral

FDA product code KOE · 27 cleared devices

Class 2 Gastroenterology, Urology
Regulation
21 CFR 876.5520
Review panel
GU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1979-12-06 – 2020-01-02
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