FDA 510(k) Application Details - K962333

Device Classification Name	Resin, Denture, Relining, Repairing, Rebasing   More FDA Info for this Device
510(K) Number	K962333
Device Name	Resin, Denture, Relining, Repairing, Rebasing
Applicant	VIDENT 3150 EAST BIRCH ST. BREA, CA 92821 US Other 510(k) Applications for this Company
Contact	RAY E MORROW Other 510(k) Applications for this Contact
Regulation Number	872.3760   More FDA Info for this Regulation Number
Classification Product Code	EBI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/1996
Decision Date	08/07/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review