FDA 510(k)

Lilium a-200E

K-Number: K170046 · 2017-12-07

Decision Date2017-12-07

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Lilium a-200E is the device name listed in this FDA 510(k) record. The listed applicant is Lilium Otsuka Co., Ltd.. It received FDA 510(k) clearance on 2017-12-07 under 510(k) 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. The listed applicant is Lilium Otsuka Co., Ltd.. The 510(k) number is K170046.

When did Lilium a-200E receive FDA 510(k) clearance?

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

Who is the listed applicant for Lilium a-200E?

The FDA 510(k) record lists Lilium Otsuka Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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