FDA 510(k) Application Details - K152180

Device Classification Name	Material, Impression   More FDA Info for this Device
510(K) Number	K152180
Device Name	Material, Impression
Applicant	Neosil Co., Ltd 63, Gongdanseoro 18 beon-gil, Geumjeong-gu Busan 609-809 KR Other 510(k) Applications for this Company
Contact	Park Dong Min 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	08/04/2015
Decision Date	10/22/2015
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