FDA 510(k) Premarket Notification K150975: Philips IntelliVue MP2/MP5/MPSC Patient Monitors, Philips IntelliVue X1 and X2 multi-msrmt-modules for use with IntelliVue patient monitors

Submission Details & Decision

Normalized public record details for 510(k) notification K150975.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K150975

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

Philips IntelliVue MP2/MP5/MPSC Patient Monitors, Philips IntelliVue X1 and X2 multi-msrmt-modules for use with IntelliVue patient monitors

Product Code

MHX

Decision Date

2015-06-25

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Special

Third Party Flag

Date Received

2015-04-13

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