FDA 510(k) Application Details - K210970

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K210970
Device Name	Mask, Surgical
Applicant	BYD Precison Manufacturer Co., Ltd. No.3001 Baohe Road, Baolong Industrial Area, Longgang Shenzhen 518116 CN Other 510(k) Applications for this Company
Contact	Yubo Guan 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	03/31/2021
Decision Date	07/21/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review