FDA 510(k) Application Details - K982201

Device Classification Name	Material, Tooth Shade, Resin   More FDA Info for this Device
510(K) Number	K982201
Device Name	Material, Tooth Shade, Resin
Applicant	FOREMOST DENTAL MFG., INC. 242 SOUTH DEAN ST. ENGLEWOOD, NJ 07631 US Other 510(k) Applications for this Company
Contact	D T WOLF Other 510(k) Applications for this Contact
Regulation Number	872.3690   More FDA Info for this Regulation Number
Classification Product Code	EBF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/22/1998
Decision Date	08/10/1998
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