FDA 510(k)

PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50

K-Number: K040304 · 2004-03-01

ApplicantPhilips Medizin Systeme Boeblingen GmbH

Decision Date2004-03-01

Product CodeMHX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. It received FDA 510(k) clearance on 2004-03-01 under 510(k) number K040304. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50?

PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50 is a medical device that received FDA 510(k) clearance on 2004-03-01. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K040304.

When did PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50 receive FDA 510(k) clearance?

PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50 received FDA 510(k) clearance on 2004-03-01, under 510(k) number K040304.

Who is the listed applicant for PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50?

The FDA 510(k) record lists Philips Medizin Systeme Boeblingen GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50?

The FDA product code for PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50 is MHX.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.