K231671
- 510(k) number
- K231671
- Device name
- IntelliVue Patient Monitor MX750 (866471), IntelliVue Patient Monitor MX850 (866470), IntelliVue 4-Slot Module Rack FMX-4 (866468)
- Applicant
- Philips Medizin Systeme Boeblingen GmbH DE
- Product code
- MHX — Monitor, Physiological, Patient(With Arrhythmia Dete
- Decision date
- 2023-12-19
- Date received
- 2023-06-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K231671.pdf
Official FDA record: K231671
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.