FDA 510(k) Application Details - K102173

Device Classification Name	Respirator,Surgical   More FDA Info for this Device
510(K) Number	K102173
Device Name	Respirator,Surgical
Applicant	MOLDEX/METRIC, INC. 10111 WEST JEFFERSON BLVD. CULVER CITY, CA 90232 US Other 510(k) Applications for this Company
Contact	MARK MEINECKE Other 510(k) Applications for this Contact
Regulation Number	878.4040   More FDA Info for this Regulation Number
Classification Product Code	MSH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/02/2010
Decision Date	09/13/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	Y
Expedited Review