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FDA 510(k)

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)

K-Number: K233877 · 2024-03-04

ApplicantMagic Mobility
Decision Date2024-03-04
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) is a medical device manufactured by Magic Mobility. It received FDA 510(k) clearance on 2024-03-04 under approval number K233877. 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 XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)?

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) is a medical device that received FDA 510(k) clearance on 2024-03-04. It is manufactured by Magic Mobility. The 510(k) number is K233877.

When was XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) approved by the FDA?

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) received FDA 510(k) clearance on 2024-03-04, under approval number K233877.

What company makes XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)?

XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) is manufactured by Magic Mobility.

What is the FDA product code for XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4)?

The FDA product code for XT Series Power Wheelchair (XT2), XT Series Power Wheelchair (XT4) is ITI.

Other Devices by Magic Mobility

K213090Frontier Series Power Wheelchairs K211574Extreme X8 K203083Magic 360 Power Wheelchair

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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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