FDA 510(k) Application Details - K151748

Device Classification Name	More FDA Info for this Device
510(K) Number	K151748
Device Name	Clean & More
Applicant	3M DEUTSCHLAND GMBH ESPE PLATZ SEEFELD 82234 DE Other 510(k) Applications for this Company
Contact	DESI W SOEGIARTO Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PIP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/29/2015
Decision Date	03/11/2016
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