FDA 510(k)

PHILIPS MP5 INTELLIVUE PATIENT MONITOR

K-Number: K062392 · 2006-09-06

ApplicantPhilips Medizin Systeme Boeblingen GmbH

Decision Date2006-09-06

Product CodeMHX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PHILIPS MP5 INTELLIVUE PATIENT MONITOR 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 2006-09-06 under 510(k) number K062392. 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 MP5 INTELLIVUE PATIENT MONITOR?

PHILIPS MP5 INTELLIVUE PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 2006-09-06. The listed applicant is Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K062392.

When did PHILIPS MP5 INTELLIVUE PATIENT MONITOR receive FDA 510(k) clearance?

PHILIPS MP5 INTELLIVUE PATIENT MONITOR received FDA 510(k) clearance on 2006-09-06, under 510(k) number K062392.

Who is the listed applicant for PHILIPS MP5 INTELLIVUE PATIENT MONITOR?

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 MP5 INTELLIVUE PATIENT MONITOR?

The FDA product code for PHILIPS MP5 INTELLIVUE PATIENT MONITOR is MHX.

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Related Devices (Code: 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.