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FDA 510(k), K792042, DENTURE BASE RESIN
FDA 510(k), K792042, DENTURE BASE RESIN
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510(K) Number: K792042
Device Name: DENTURE BASE RESIN
Manufacturer:
Device Classification Name: Resin, Denture, Relining, Repairing, Rebasing
Regulation Number: EBI
Classification Product Code: 10/12/1979
Date Received: 11/30/1979
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
Device Name: DENTURE BASE RESIN
Manufacturer:
Device Classification Name: Resin, Denture, Relining, Repairing, Rebasing
Regulation Number: EBI
Classification Product Code: 10/12/1979
Date Received: 11/30/1979
Decision Date: Substantially Equivalent (SESE)
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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