FDA 510(k) Application Details - K203012

Device Classification Name	Mask, Surgical   More FDA Info for this Device
510(K) Number	K203012
Device Name	Mask, Surgical
Applicant	Customfab, INC. 7345 Orangewood Ave Garden Grove, CA 92841 US Other 510(k) Applications for this Company
Contact	Erentia Gillmer 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	10/01/2020
Decision Date	04/11/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review