FDA 510(k) Application Details - K963862

Device Classification Name	Tester, Pulp   More FDA Info for this Device
510(K) Number	K963862
Device Name	Tester, Pulp
Applicant	SYBRON DENTAL SPECIALTIES, INC. 1717 WEST COLLINS AVE. ORANGE, CA 92667 US Other 510(k) Applications for this Company
Contact	COLLEEN BOSWELL Other 510(k) Applications for this Contact
Regulation Number	872.1720   More FDA Info for this Regulation Number
Classification Product Code	EAT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/24/1996
Decision Date	12/02/1996
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