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Remover, Intrauterine Device, Contraceptive, Hook-Type

FDA product code HHF · 6 cleared devices

Class 1 Obstetrics/Gynecology
Regulation
21 CFR 884.4530
Review panel
OB
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1981-09-21 – 1994-02-24
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