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Speculum, Vaginal, Metal, Fiberoptic

FDA product code HDG · 2 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
1977-07-14 – 1987-01-09
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