FDA 510(k) Application Details - K200923

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K200923
Device Name	Mask, Surgical
Applicant	BYD Precision 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	04/07/2020
Decision Date	08/26/2020
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