FDA 510(k) Application Details - K210748

Device Classification Name	Needle, Hypodermic, Single Lumen   More FDA Info for this Device
510(K) Number	K210748
Device Name	Needle, Hypodermic, Single Lumen
Applicant	W. L. Med Co., Ltd. 246, Geumgwangosan-ro, Geumgwang-yeon Anseong-si 17535 KR Other 510(k) Applications for this Company
Contact	Ha Tae Joo 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	03/12/2021
Decision Date	05/25/2022
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