FDA 510(k) Applications Submitted by Teresa Davidson

FDA 510(k) Number	Submission Date	Device Name	Applicant
K010912	03/27/2001	ALARMVIEW WIRELESS DATA NETWORK SYSTEM	DATA CRITICAL CORP.
K211947	06/23/2021	GlideScope BFlex 2.8 Single-Use Bronchoscope	Verathon Medical (Canada) ULC
K011999	06/27/2001	MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM	DATA CRITICAL CORP.
K012005	06/27/2001	MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM	DATA CRITICAL CORP.
K013156	09/21/2001	MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM	DATA CRITICAL CORP.
K102757	09/23/2010	LIFENET SYSTEM	PHYSIO-CONTROL, INC.
K082937	10/01/2008	LIFEPAK 15 MONITOR/DEFIBRILLATOR	PHYSIO-CONTROL, INC.
K052854	10/11/2005	LIFENET EXCHANGE SYSTEM	MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC.
K123597	11/21/2012	TRUECPR COACHING DEVICE	PHYSIO-CONTROL, INC.
K183256	11/21/2018	GlideScope BFlex Single-Use Bronchoscope System	Verathon Medical (Canada) ULC
K193488	12/17/2019	GlideScope BFlex 3.8 Single-Use Bronchoscope	Verathon Medical (Canada) ULC
K093925	12/22/2009	LIFENET SYSTEM	PHYSIO-CONTROL, INC.
K003998	12/26/2000	FLEXVIEW CLINICAL MONITORING SYSTEM	DATA CRITICAL CORP.