FDA 510(k) Application Details - K133493

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K133493
Device Name	Syringe, Piston
Applicant	JIANGXI KELUN MEDICAL DEVICES MANUFACTURING CO.,LT ROOM 302, NO.21 BUILDING KAIYU GARDEN, XISHAN SOUTH ROAD WENZHOU 325000 CN Other 510(k) Applications for this Company
Contact	HELEN NAN Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	FMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/14/2013
Decision Date	03/27/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review