FDA 510(k) Application Details - K220333

Device Classification Name	Gown, Surgical   More FDA Info for this Device
510(K) Number	K220333
Device Name	Gown, Surgical
Applicant	Medline Industries, LP. Three Lakes Drive Northfield, IL 60093 US Other 510(k) Applications for this Company
Contact	Adam Ostrower Other 510(k) Applications for this Contact
Regulation Number	878.4040   More FDA Info for this Regulation Number
Classification Product Code	FYA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/04/2022
Decision Date	05/18/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review