FDA 510(k) Application Details - K131879

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K131879
Device Name	Mask, Surgical
Applicant	KIMBERLY-CLARK CORP. 1400 HOLCOMB BRIDGE RD. ROSWELL, GA 30076 US Other 510(k) Applications for this Company
Contact	MONICA KING Other 510(k) Applications for this Contact
Regulation Number	878.4040   More FDA Info for this Regulation Number
Classification Product Code	FXX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/24/2013
Decision Date	12/20/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review