IntelliVue Multi-Measurement Module MMX
K-Number: K181831 · 2018-11-15
Device Summary
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.
Related Clinical Trials
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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.