FDA 510(k) Application Details - K012740

Device Classification Name	Material, Tooth Shade, Resin   More FDA Info for this Device
510(K) Number	K012740
Device Name	Material, Tooth Shade, Resin
Applicant	KURARAY MEDICAL INC. 30TH FL. METLIFE BUILDING 200 PARK AVENUE NEW YORK, NY 10166 US Other 510(k) Applications for this Company
Contact	MASAYA SASAKI 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	08/14/2001
Decision Date	09/14/2001
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