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Insufflator, Carbon-Dioxide, Uterotubal (And Accessories)

FDA product code HES · 12 cleared devices

Class 2 Obstetrics/Gynecology
Regulation
21 CFR 884.1300
Review panel
OB
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1984-07-03 – 2000-04-19
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