FDA 510(k), K955822, REMOVABLE HERBST APPLIANCE

FDA 510(k), K955822, REMOVABLE HERBST APPLIANCE

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510(K) Number: K955822
Device Name: REMOVABLE HERBST APPLIANCE
Manufacturer: UNIV. DENTAL ASSOC. DEPARTMENT OF ORTHODONTICS
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 12/26/1995
Decision Date: 03/20/1996
Regulation Medical Specialty: Dental

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