K251702
- 510(k) number
- K251702
- Device name
- IntelliVue Patient Monitor MX750; IntelliVue Patient Monitor MX850; IntelliVue 4-Slot Module Rack FMX-4 (866471 866470 866468 )
- Applicant
- Philips Medizin Systeme Böblingen GmbH DE
- Product code
- MHX — Monitor, Physiological, Patient(With Arrhythmia Dete
- Decision date
- 2025-11-10
- Date received
- 2025-06-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K251702.pdf
Official FDA record: K251702
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.