FDA 510(k) Premarket Notification K040304: PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50

Submission Details & Decision

Normalized public record details for 510(k) notification K040304.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K040304

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50

Product Code

MHX

Decision Date

2004-03-01

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Special

Third Party Flag

Date Received

2004-02-09

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