FDA 510(k) Application Details - K180259

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K180259
Device Name	Needle, Hypodermic, Single Lumen
Applicant	Jiangsu Shenli Medical Production Co., Ltd No 20, Changzheng Road, Zhenglu Changzhou City 213111 CN Other 510(k) Applications for this Company
Contact	Tina Cai Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	FMI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/30/2018
Decision Date	05/18/2018
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