FDA 510(k), K023836, THE SUAD DEVICE

FDA 510(k), K023836, THE SUAD DEVICE

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510(K) Number: K023836
Device Name: THE SUAD DEVICE
Manufacturer: STRONG DENTAL INC.
Device Classification Name: device, anti-snoring
Regulation Number: 872.5570
Classification Product Code: LRK
Date Received: 11/18/2002
Decision Date: 07/08/2003
Regulation Medical Specialty: Dental
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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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