FDA 510(k) Applications Submitted by TIMOTHY HOLWICK

FDA 510(k) Number	Submission Date	Device Name	Applicant
K160718	03/15/2016	Vital Sync Informatics Manager & Virtual Patient Monitoring Platform	COVIDIEN
K130889	03/29/2013	SPLIT CATH RG	MEDCOMP
K141151	05/05/2014	CT MIDLINE	MEDCOMP (MEDICAL COMPONENTS, INC.)
K132498	08/09/2013	VALVED TEARAWAY INTRODUCER GENERATION II	MEDCOMP (MEDICAL COMPONENTS, INC.)
K132880	09/13/2013	MEDCOMP POWER INJECTABLE SAFETY HUBER NEEDLE	MEDICAL COMPONENTS INC
K123292	10/22/2012	T3	MEDCOMP
K143506	12/10/2014	BIS STANDARD SENSOR,1-CHANNEL (3 ELECTRODES); BIS PEDI SENSOR,1-CHANNEL,3 ELECTRODES; BIS QUATRO SENSOR; BIS PEDI-XP SENSOR,2-CHANNEL (4 ELECTRODES); BIS EXTEND SENSOR; BIS BILATERAL SENSOR,4-CHANNEL (6 ELECRODES); BIS INSIGHT SENSOR,CVI-ENABLED,2-CHANNEL	COVIDIEN
K124046	12/31/2012	VALVED TEARAWAY INTRODUCER GENERATION II	MEDICAL COMPONENTS INC