FDA 510(k) Application Details - K072851

Device Classification Name	Resin, Denture, Relining, Repairing, Rebasing   More FDA Info for this Device
510(K) Number	K072851
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	DEVON O HOWE 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	10/04/2007
Decision Date	02/20/2008
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