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FDA 510(k)

Luggie Chair

K-Number: K160139 · 2017-03-20

ApplicantFreerider Corporation
Decision Date2017-03-20
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Luggie Chair is a medical device manufactured by Freerider Corporation. It received FDA 510(k) clearance on 2017-03-20 under approval number K160139. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Luggie Chair?

Luggie Chair is a medical device that received FDA 510(k) clearance on 2017-03-20. It is manufactured by Freerider Corporation. The 510(k) number is K160139.

When was Luggie Chair approved by the FDA?

Luggie Chair received FDA 510(k) clearance on 2017-03-20, under approval number K160139.

What company makes Luggie Chair?

Luggie Chair is manufactured by Freerider Corporation.

What is the FDA product code for Luggie Chair?

The FDA product code for Luggie Chair is ITI.

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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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