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FDA 510(k)

M3290B Philips IntelliVue Information Center iX

K-Number: K163584 · 2017-07-07

Decision Date2017-07-07
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

M3290B Philips IntelliVue Information Center iX is a medical device manufactured by Philips Medical Systems. It received FDA 510(k) clearance on 2017-07-07 under approval number K163584. 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 M3290B Philips IntelliVue Information Center iX?

M3290B Philips IntelliVue Information Center iX is a medical device that received FDA 510(k) clearance on 2017-07-07. It is manufactured by Philips Medical Systems. The 510(k) number is K163584.

When was M3290B Philips IntelliVue Information Center iX approved by the FDA?

M3290B Philips IntelliVue Information Center iX received FDA 510(k) clearance on 2017-07-07, under approval number K163584.

What company makes M3290B Philips IntelliVue Information Center iX?

M3290B Philips IntelliVue Information Center iX is manufactured by Philips Medical Systems.

What is the FDA product code for M3290B Philips IntelliVue Information Center iX?

The FDA product code for M3290B Philips IntelliVue Information Center iX is MHX.

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Official Source

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