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Illuminator, Fiberoptic, Surgical Field

FDA product code HBI · 27 cleared devices

Class 2 General, Plastic Surgery
Regulation
21 CFR 878.4580
Review panel
SU
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
1981-02-27 – 2023-01-13
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