FDA 510(k) Application Details - K222417

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K222417
Device Name	Needle, Hypodermic, Single Lumen
Applicant	Shina Corporation 8-26, Bojeokdong-gil Gongju 32533 KR Other 510(k) Applications for this Company
Contact	Seunggi Jeon 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	08/10/2022
Decision Date	03/20/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review