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FDA 510(k)

Illumeo System

K-Number: K173588 · 2018-01-12

ApplicantPhilips Medical Systems Technologies , Ltd.
Decision Date2018-01-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Illumeo System is a medical device manufactured by Philips Medical Systems Technologies , Ltd.. It received FDA 510(k) clearance on 2018-01-12 under approval number K173588. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Illumeo System?

Illumeo System is a medical device that received FDA 510(k) clearance on 2018-01-12. It is manufactured by Philips Medical Systems Technologies , Ltd.. The 510(k) number is K173588.

When was Illumeo System approved by the FDA?

Illumeo System received FDA 510(k) clearance on 2018-01-12, under approval number K173588.

What company makes Illumeo System?

Illumeo System is manufactured by Philips Medical Systems Technologies , Ltd..

What is the FDA product code for Illumeo System?

The FDA product code for Illumeo System is LLZ.

Other Devices by Philips Medical Systems Technologies , Ltd.

K240844Spectral CT 7500 RT K244008Spectral CT K253649Spectral CT Verida Family

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Official Source

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