FDA 510(k) Application Details - K210348

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K210348
Device Name	Mask, Surgical
Applicant	Weihai Dishang Medical Technology Co., Ltd Room 406-409, Block C, No.213 Torch Road, Torch High-Tech Industrial Development Zone Weihai 264209 CN Other 510(k) Applications for this Company
Contact	Ricky Xia 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	02/08/2021
Decision Date	10/24/2021
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