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FDA 510(k), K831793, AQUALIZER MOUTHPIECE
FDA 510(k), K831793, AQUALIZER MOUTHPIECE
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510(K) Number: K831793
Device Name: AQUALIZER MOUTHPIECE
Manufacturer: MARTIN D. LERMAN
Device Classification Name: positioner, tooth, preformed
Regulation Number: 872.5525
Classification Product Code: KMY
Date Received: 06/03/1983
Decision Date: 08/12/1983
Regulation Medical Specialty: Dental
Device Name: AQUALIZER MOUTHPIECE
Manufacturer: MARTIN D. LERMAN
Device Classification Name: positioner, tooth, preformed
Regulation Number: 872.5525
Classification Product Code: KMY
Date Received: 06/03/1983
Decision Date: 08/12/1983
Regulation Medical Specialty: Dental
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- 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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