FDA 510(k) Applications Submitted by Philips Medizin Systeme B÷blingen GmbH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K241556	05/31/2024	Cardiac Workstation (5000); Cardiac Workstation (7000)	Philips Medizin Systeme B÷blingen GmbH
K241890	06/28/2024	Philips Holter Analysis System	Philips Medizin Systeme B÷blingen GmbH
K242962	09/25/2024	Telemetry Monitor 5500 Release 4.0 (867232)	Philips Medizin Systeme B÷blingen GmbH
K243545	11/15/2024	Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name: 989803170171, OR 3-Lead ECG Trunk Cable, AAMI/IEC; 989803170181, OR 5-Lead ECG Trunk Cable, AAMI/IEC; M1667A, 6 Lead ECG Trunk, AAMI/IEC 2.7m; M1668A,5 Lead ECG Trunk, AAMI/IEC	Philips Medizin Systeme B÷blingen GmbH
K211900	06/21/2021	Patient Information Center iX	Philips Medizin Systeme B÷blingen GmbH
K221348	05/09/2022	IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470)	Philips Medizin Systeme B÷blingen GmbH