FDA 510(k) Application Details - K230447

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K230447
Device Name	Syringe, Piston
Applicant	Shanghai Kindly Enterprise Development Group Co., Ltd No.658 Gaochao Road Shanghai 201803 CN Other 510(k) Applications for this Company
Contact	Hualong Liu 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	02/21/2023
Decision Date	08/16/2023
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