FDA 510(k) Application Details - K033521

Device Classification Name	Liner, Cavity, Calcium Hydroxide   More FDA Info for this Device
510(K) Number	K033521
Device Name	Liner, Cavity, Calcium Hydroxide
Applicant	BISCO, INC. 1100 WEST IRVING PARK RD. SCHAUMBURG, IL 60193 US Other 510(k) Applications for this Company
Contact	BENJAMIN LICHTENWALNER Other 510(k) Applications for this Contact
Regulation Number	872.3250   More FDA Info for this Regulation Number
Classification Product Code	EJK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/07/2003
Decision Date	01/16/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review