FDA 510(k) Application Details - K140966

Device Classification Name	Material, Impression   More FDA Info for this Device
510(K) Number	K140966
Device Name	Material, Impression
Applicant	VERICOM CO., LTD. 48, Toegyegongdan 1-gil Chuncheon-Si, Gangwon - Do 200-944 KR Other 510(k) Applications for this Company
Contact	Myung-Hwan Oh Other 510(k) Applications for this Contact
Regulation Number	872.3660   More FDA Info for this Regulation Number
Classification Product Code	ELW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/15/2014
Decision Date	08/15/2014
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