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Holder, Speculum, Ent

FDA product code KAG · 2 cleared devices

Class 1 General, Plastic Surgery
Regulation
21 CFR 878.1800
Review panel
SU
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1983-01-08 – 1984-09-21
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