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FDA 510(k)

IntelliVue Multi-Measurement Module MMX

K-Number: K181831 · 2018-11-15

Decision Date2018-11-15
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IntelliVue Multi-Measurement Module MMX is a medical device manufactured by Philips Medizin Systeme Boeblingen GmbH. It received FDA 510(k) clearance on 2018-11-15 under approval number K181831. 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 IntelliVue Multi-Measurement Module MMX?

IntelliVue Multi-Measurement Module MMX is a medical device that received FDA 510(k) clearance on 2018-11-15. It is manufactured by Philips Medizin Systeme Boeblingen GmbH. The 510(k) number is K181831.

When was IntelliVue Multi-Measurement Module MMX approved by the FDA?

IntelliVue Multi-Measurement Module MMX received FDA 510(k) clearance on 2018-11-15, under approval number K181831.

What company makes IntelliVue Multi-Measurement Module MMX?

IntelliVue Multi-Measurement Module MMX is manufactured by Philips Medizin Systeme Boeblingen GmbH.

What is the FDA product code for IntelliVue Multi-Measurement Module MMX?

The FDA product code for IntelliVue Multi-Measurement Module MMX is MHX.

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Official Source

View on FDA Database →

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