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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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