FDA 510(k) Application Details - K960799

Device Classification Name	Tester, Pulp   More FDA Info for this Device
510(K) Number	K960799
Device Name	Tester, Pulp
Applicant	ULTIMATE WIREFORMS, INC. 200 CENTRAL ST. BRISTOL, CT 06010 US Other 510(k) Applications for this Company
Contact	DONALD F PELLETIER 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	02/27/1996
Decision Date	05/09/1996
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