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Monitor, Pressure, Intrauterine

FDA product code KXO · 26 cleared devices

Class 2 Obstetrics/Gynecology
Regulation
21 CFR 884.2700
Review panel
OB
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1979-03-21 – 1999-07-08
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