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FDA 510(k)

Lilium a-200E

K-Number: K170046 · 2017-12-07

ApplicantLilium Otsuka Co., Ltd.
Decision Date2017-12-07
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Lilium a-200E is a medical device manufactured by Lilium Otsuka Co., Ltd.. It received FDA 510(k) clearance on 2017-12-07 under approval number K170046. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lilium a-200E?

Lilium a-200E is a medical device that received FDA 510(k) clearance on 2017-12-07. It is manufactured by Lilium Otsuka Co., Ltd.. The 510(k) number is K170046.

When was Lilium a-200E approved by the FDA?

Lilium a-200E received FDA 510(k) clearance on 2017-12-07, under approval number K170046.

What company makes Lilium a-200E?

Lilium a-200E is manufactured by Lilium Otsuka Co., Ltd..

What is the FDA product code for Lilium a-200E?

The FDA product code for Lilium a-200E is IYO.

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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.

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