FDA 510(k) Applications Submitted by BRYAN HANN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K162843	10/11/2016	Small (4) Roller Pump for the Terumo Advanced Perfusion System 1, Large (6) Roller Pump for the Terumo Advanced Perfusion System 1	Terumo Cardiovascular Systems Corporation
K153376	11/23/2015	Advanced Perfusion System 1	Terumo Cardiovascular Systems Corporation
K163531	12/16/2016	Advanced Perfusion System 1	TERUMO CARDIOVASCULAR SYSTEMS CORPORATION
K212194	07/14/2021	Stryker Q Guidance System with Cranial Guidance Software, CranialMask Tracker and Microscope Tracker, Passive Optical Navigation Instruments, Mayfield Base with Articulating Arm, and Navigated Biopsy Needle, Electromagnetic Navigation Instruments, Precisi	Stryker Corporation
K172220	07/24/2017	Advanced Perfusion System 1	Terumo Cardiovascular Systems Corporation
K182110	08/06/2018	CDI Blood Parameter Monitoring System 550	Terumo Cardiovascular Systems Corporation