Philips Medizin Systeme Böblingen GmbH
Philips Medizin Systeme Böblingen GmbH holds FDA 510(k) medical device clearances, first cleared 2022, most recent 2026.
Top product codes for Philips Medizin Systeme Böblingen GmbH
Recent clearances by Philips Medizin Systeme Böblingen GmbH
- K252821 — Reusable Adult SpO2 Clip Sensor (3m) (M1196A); Reusable Adult SpO2 Clip Sensor (0.9m) (M1196T)
- K253654 — IntelliVue Measurement Rack 6000 (867317)
- K251702 — IntelliVue Patient Monitor MX750 +2 more
- K250453 — IntelliVue Patient Monitor 6100 (6100); IntelliVue Patient Monitor 6300 (6300); IntelliVue Patient Monitor 6500 (6500)
- K242962 — Telemetry Monitor 5500 Release 4.0 (867232)
- K241890 — Philips Holter Analysis System
- K243545 — Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name: 989803170171, OR 3-Lead ECG Trunk Cable, AAMI/IEC +9 more
- K241556 — Cardiac Workstation (5000); Cardiac Workstation (7000)
- K221348 — IntelliVue Patient Monitor MX750 (866471); IntelliVue Patient Monitor MX850 (866470)
- K211900 — Patient Information Center iX
Data sourced from openFDA. This site is unofficial and independent of the FDA.