FDA 510(k)

THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20

K-Number: K031481 · 2003-05-29

ApplicantPhilips Medizin Systeme Boblingen GmbH

Decision Date2003-05-29

Product CodeMHX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medizin Systeme Boblingen GmbH. It received FDA 510(k) clearance on 2003-05-29 under 510(k) number K031481. 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 THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20?

THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20 is a medical device that received FDA 510(k) clearance on 2003-05-29. The listed applicant is Philips Medizin Systeme Boblingen GmbH. The 510(k) number is K031481.

When did THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20 receive FDA 510(k) clearance?

THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20 received FDA 510(k) clearance on 2003-05-29, under 510(k) number K031481.

Who is the listed applicant for THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20?

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

What is the FDA product code for THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20?

The FDA product code for THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20 is MHX.

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Official Source

View on FDA Database →

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