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Applicator, Absorbent Tipped, Non-Sterile

FDA product code KXF · 21 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
Yes
Clearance span
1977-04-15 – 2012-12-19
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