FDA 510(k) Premarket Notification K252726: IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036)

Submission Details & Decision

Normalized public record details for 510(k) notification K252726.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K252726

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036)

Product Code

MHX

Decision Date

2026-02-06

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Traditional

Third Party Flag

Date Received

2025-08-28

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