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Instrument, Manual, General Obstetric-Gynecologic

FDA product code KOH · 15 cleared devices

Class 1 Obstetrics/Gynecology
Regulation
21 CFR 884.4520
Review panel
OB
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1978-06-28 – 2000-04-21
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