FDA 510(k) Application Details - K964191

Device Classification Name	Liner, Cavity, Calcium Hydroxide   More FDA Info for this Device
510(K) Number	K964191
Device Name	Liner, Cavity, Calcium Hydroxide
Applicant	SYBRON DENTAL SPECIALTIES, INC. 1717 WEST COLLINS AVE. ORANGE, CA 92867 US Other 510(k) Applications for this Company
Contact	WILLIAM R PIKE 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	10/21/1996
Decision Date	01/22/1997
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