FDA 510(k) Applications Submitted by Gregory Land

FDA 510(k) Number	Submission Date	Device Name	Applicant
K200446	02/24/2020	STERIS Patient Warming System	STERIS Corporation
K230558	02/28/2023	Revital-Ox PAA High Level Disinfectant Chemical Indicator	STERIS Corporation
K230560	02/28/2023	enspire 300 Series Automated Endoscope Reprocessor System	STERIS Corporation
K231490	05/23/2023	Celerity 20 HP Biological Indicator; VERIFY V24 Self-Contained Biological Indicator	STERIS Corporation
K231746	06/15/2023	VERIFY Spore Test Strip for S40 Sterilant Concentrate	Steris Corporation
K181865	07/12/2018	Acu-sInQ Complete Endoscope Cleaning Aid System	STERIS Corporation
K192020	07/29/2019	Celerity HP Chemical Indicator, Celerity Vaporized VH2O2 Process Indicator Adhesive Label, VERIFY V24 Self-Contained Biological Indicator Vial Label	STERIS Corporation
K192518	09/13/2019	Reusable Monopolar Active Cord	US Endoscopy
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
K223717	12/12/2022	Celerity 5 HP Biological Indicator; Celerity 5 HP Challenge Pack	STERIS Corporation
K213881	12/13/2021	Celerity Incubator	STERIS Corporation