FDA 510(k) Application Details - K081241

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K081241
Device Name	Syringe, Piston
Applicant	SHANDONG WEIGAO GROUP MEDICAL POLYMER CO.,LTD. SUITE 8D, NO.19, LANE 999 ZHONGSHAN NO.2 ROAD(S) SHANGHAI 200030 CN Other 510(k) Applications for this Company
Contact	Diana Hong 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	05/01/2008
Decision Date	09/08/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review