FDA 510(k) Application Details - K143155

Device Classification Name	Varnish, Cavity   More FDA Info for this Device
510(K) Number	K143155
Device Name	Varnish, Cavity
Applicant	Johnson & Johnson Healthcare Products, Division of McNeil-PP 199 Grandview Road Skillman, NJ 08558 US Other 510(k) Applications for this Company
Contact	ANGELINA M. HUNT Other 510(k) Applications for this Contact
Regulation Number	872.3260   More FDA Info for this Regulation Number
Classification Product Code	LBH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/03/2014
Decision Date	01/29/2015
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