FDA 510(k) Application Details - K211771

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K211771
Device Name	Mask, Surgical
Applicant	The GOOD Corporation 47-13 Eoso 3-gil, Cheongbuk-eup Pyeongtaek-si 17795 KR Other 510(k) Applications for this Company
Contact	Hak Rae Lee 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	06/08/2021
Decision Date	08/24/2022
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