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Stent, Vaginal

FDA product code KXP · 4 cleared devices

Class 2 Obstetrics/Gynecology
Regulation
21 CFR 884.3900
Review panel
OB
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1995-11-08 – 2020-09-30
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