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Device, Anti-Stammering

FDA product code KTH · 4 cleared devices

Class 1 Ear, Nose, Throat
Regulation
21 CFR 874.5840
Review panel
EN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
1980-03-12 – 1996-09-09
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