FDA 510(k) Application Details - K211827

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K211827
Device Name	Mask, Surgical
Applicant	Zhejiang Lanhine Medical Products LTD 1989 Cidong Road, Cidongbinhai District Cixi 315300 CN Other 510(k) Applications for this Company
Contact	Jerry Gu 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	06/14/2021
Decision Date	09/23/2021
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