FDA 510(k) Application Details - K234024

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K234024
Device Name	Syringe, Piston
Applicant	Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd No. 2 Guanyin Road, Taihu Economic Development Zone Anqing 246400 CN Other 510(k) Applications for this Company
Contact	Bingyi Xiang 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	12/20/2023
Decision Date	03/19/2024
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