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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 the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Technologies , Ltd.. It received FDA 510(k) clearance on 2018-01-12 under 510(k) 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. The listed applicant is Philips Medical Systems Technologies , Ltd.. The 510(k) number is K173588.

When did Illumeo System receive FDA 510(k) clearance?

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

Who is the listed applicant for Illumeo System?

The FDA 510(k) record lists Philips Medical Systems Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Illumeo System?

The FDA product code for Illumeo System is LLZ.

Other records listing Philips Medical Systems Technologies , Ltd. as applicant

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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.

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