FDA 510(k) Application Details - K133298

Device Classification Name	Handpiece, Direct Drive, Ac-Powered   More FDA Info for this Device
510(K) Number	K133298
Device Name	Handpiece, Direct Drive, Ac-Powered
Applicant	META BIOMED, INC. 2600 MULLINIX MILL ROAD MT. AIRY, MD 21771 US Other 510(k) Applications for this Company
Contact	BLIX WINSTON Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EKX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/25/2013
Decision Date	09/19/2014
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