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Recorder, Pressure, Intrauterine

FDA product code HFO · 4 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
1978-05-09 – 1997-11-12
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