Philips Medizin Systeme B?blingen GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Philips Medizin Systeme B?blingen GmbH - FDA 510(k) Cleared Devices
Recent clearances: Reusable Adult SpO2 Clip Sensor (3m) (M1196A), IntelliVue Patient Monitor MX750, IntelliVue Patient Monitor 6100 (6100)
9
Total
9
Cleared
0
Denied
Philips Medizin Systeme B?blingen GmbH has 9 FDA 510(k) cleared medical devices. Based in Boeblingen, DE.
Latest FDA clearance: May 2026. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Philips Medizin Systeme B?blingen GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Philips Medizin Systeme Böblingen GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Philips Medizin Systeme B?blingen GmbH
9 devices
Cleared
May 29, 2026
Reusable Adult SpO2 Clip Sensor (3m) (M1196A)
Anesthesiology
267d
Cleared
Nov 10, 2025
IntelliVue Patient Monitor MX750
Cardiovascular
161d
Cleared
Sep 02, 2025
IntelliVue Patient Monitor 6100 (6100)
Cardiovascular
196d
Cleared
May 05, 2025
Telemetry Monitor 5500 Release 4.0 (867232)
Cardiovascular
222d
Cleared
Mar 21, 2025
Philips Holter Analysis System
Cardiovascular
266d
Cleared
Jan 17, 2025
Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name:...
Cardiovascular
63d
Cleared
Dec 17, 2024
Cardiac Workstation (5000)
Cardiovascular
200d
Cleared
Feb 03, 2023
IntelliVue Patient Monitor MX750 (866471)
Cardiovascular
270d
Cleared
Mar 04, 2022
Patient Information Center iX
Cardiovascular
256d