FDA 510(k) Application Details - K033020

Device Classification Name	Resin, Denture, Relining, Repairing, Rebasing   More FDA Info for this Device
510(K) Number	K033020
Device Name	Resin, Denture, Relining, Repairing, Rebasing
Applicant	CMP INDUSTRIES LLC. 413 NORTH PEARL ST. ALBANY, NY 12207 US Other 510(k) Applications for this Company
Contact	WILLIAM REGAN 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	09/26/2003
Decision Date	12/19/2003
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