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Source, Carrier, Fiberoptic Light

FDA product code EQH · 49 cleared devices

Class 1 Ear, Nose, Throat
Regulation
21 CFR 874.4350
Review panel
EN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1976-12-06 – 1995-12-04
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