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Tube, Laryngectomy

FDA product code KAC · 4 cleared devices

Class 1 Ear, Nose, Throat
Regulation
21 CFR 874.4420
Review panel
EN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1981-06-16 – 1990-06-14
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