FDA 510(k) Applications Submitted by Steris Corporations

FDA 510(k) Number	Submission Date	Device Name	Applicant
K203630	12/11/2020	BioGuard Air/Water and Suction Valves	STERIS Corporations
K183295	11/27/2018	Celerity HP Chemical Indicator (CI)	Steris Corporations
K183300	11/27/2018	VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge Pack	STERIS Corporations
K190104	01/22/2019	SYSTEM 1E Liquid Chemical Sterilant Processing System, SYSTEM 1 Endo Liquid Chemical Sterilant Processing System	Steris Corporations
K180342	02/07/2018	SYSTEM 1E Liquid Chemical Sterilant Processing System	Steris Corporations
K172748	09/12/2017	VERIFY V24 Self-Contained Biological Indicator, VERIFY V24 Biological Indicator Challenge Pack	STERIS Corporations
K182931	10/22/2018	VERIFY All-In-One STEAM Reusable Test Pack, VERIFY All-In-One STEAM Reusable Test Pack with Step Counter, VERIFY All-In-One STEAM Reusable Test Pack with Tracker Tag	Steris Corporations