FDA 510(k), K091106, EQUIA

FDA 510(k), K091106, EQUIA

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510(K) Number: K091106
Device Name: EQUIA
Manufacturer: GC AMERICA, INC.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 04/16/2009
Decision Date: 06/17/2009
Regulation Medical Specialty: Dental

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