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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 the device name listed in this FDA 510(k) record. The listed applicant is Magic Mobility. It received FDA 510(k) clearance on 2021-03-17 under 510(k) 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. The listed applicant is Magic Mobility. The 510(k) number is K203083.

When did Magic 360 Power Wheelchair receive FDA 510(k) clearance?

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

Who is the listed applicant for Magic 360 Power Wheelchair?

The FDA 510(k) record lists Magic Mobility as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Magic Mobility as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: ITI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.