FDA 510(k) Application Details - K023888

Device Classification Name	Cement, Dental   More FDA Info for this Device
510(K) Number	K023888
Device Name	Cement, Dental
Applicant	GLOBAL DENTAL PRODUCTS, INC. PO BOX 537 NORTH BELLMORE, NY 11710 US Other 510(k) Applications for this Company
Contact	JERRY L BARTICK Other 510(k) Applications for this Contact
Regulation Number	872.3275   More FDA Info for this Regulation Number
Classification Product Code	EMA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/21/2002
Decision Date	03/05/2003
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