FDA 510(k)

THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90

K-Number: K061052 · 2006-05-26

ApplicantPhilips Medical Systems North America, Inc.

Decision Date2006-05-26

Product CodeMHX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America, Inc.. It received FDA 510(k) clearance on 2006-05-26 under 510(k) number K061052. 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 PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90?

THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90 is a medical device that received FDA 510(k) clearance on 2006-05-26. The listed applicant is Philips Medical Systems North America, Inc.. The 510(k) number is K061052.

When did THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90 receive FDA 510(k) clearance?

THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90 received FDA 510(k) clearance on 2006-05-26, under 510(k) number K061052.

Who is the listed applicant for THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90?

The FDA 510(k) record lists Philips Medical Systems North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90?

The FDA product code for THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90 is MHX.

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Other records listing Philips Medical Systems North America, Inc. as applicant

K102005ALLURA XPER OR TABLE SERIES K062233HEARTSTART MRX MONITOR/DEFIBRILLATOR K062283THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT MONITORS K050151MULTIDIAGNOST ELEVA K042867PHILIPS ORTHOPAEDIC APPLICATIONS K041602PANORAMA 1.0T

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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.