FDA 510(k) Application Details - K222905

Device Classification Name	Container, Sharps   More FDA Info for this Device
510(K) Number	K222905
Device Name	Container, Sharps
Applicant	Ningbo Maxcon Medical Technology Co., Ltd. No.228 Dongxin Road, Dongqiao Town Ningbo 315000 CN Other 510(k) Applications for this Company
Contact	Puhai Ma Other 510(k) Applications for this Contact
Regulation Number	880.5570   More FDA Info for this Regulation Number
Classification Product Code	MMK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/23/2022
Decision Date	06/01/2023
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