FDA 510(k)

Magic 360 Power Wheelchair

K-Number: K203083 · 2021-03-17

Decision Date2021-03-17

Product CodeITI

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Magic 360 Power Wheelchair is a medical device manufactured by Magic Mobility. It received FDA 510(k) clearance on 2021-03-17 under approval number K203083. 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 Magic 360 Power Wheelchair?

Magic 360 Power Wheelchair is a medical device that received FDA 510(k) clearance on 2021-03-17. It is manufactured by Magic Mobility. The 510(k) number is K203083.

When was Magic 360 Power Wheelchair approved by the FDA?

Magic 360 Power Wheelchair received FDA 510(k) clearance on 2021-03-17, under approval number K203083.

What company makes Magic 360 Power Wheelchair?

Magic 360 Power Wheelchair is manufactured by Magic Mobility.

What is the FDA product code for Magic 360 Power Wheelchair?

The FDA product code for Magic 360 Power Wheelchair is ITI.

Other Devices by Magic Mobility

K213090Frontier Series Power Wheelchairs K211574Extreme X8 K233877XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)

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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.