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Applicator, Absorbent Tipped, Sterile

FDA product code KXG · 1 cleared devices

Class 1 General Hospital
Regulation
21 CFR 880.6025
Review panel
HO
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1980-09-16 – 1980-09-16
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