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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: KXA
Date Received: 10/12/1979
Decision Date: 11/30/1979
Decision: 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: KXA
Date Received: 10/12/1979
Decision Date: 11/30/1979
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
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