FDA 510(k) Application Details - K202126

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K202126
Device Name	Mask, Surgical
Applicant	Shenzhen Peninsula Medical Co. Ltd B F2, Changfeng Industrial Park, XinÆan Street, BaoÆan District, Shenzhen, China Shenzhen 518100 CN Other 510(k) Applications for this Company
Contact	Zhang Sudi Other 510(k) Applications for this Contact
Regulation Number	878.4040   More FDA Info for this Regulation Number
Classification Product Code	FXX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/31/2020
Decision Date	06/08/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review