K253654
- 510(k) number
- K253654
- Device name
- IntelliVue Measurement Rack 6000 (867317)
- Applicant
- Philips Medizin Systeme Böblingen GmbH DE
- Product code
- MSX — System, Network And Communication, Physiological Mon
- Decision date
- 2026-03-30
- Date received
- 2025-11-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K253654.pdf
Official FDA record: K253654
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.