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FDA 510(k)

Power Wheelchair, W5907 (Q50 R Carbon)

K-Number: K220740 · 2022-05-12

Decision Date2022-05-12
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Power Wheelchair, W5907 (Q50 R Carbon) is a medical device manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2022-05-12 under approval number K220740. 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 Power Wheelchair, W5907 (Q50 R Carbon)?

Power Wheelchair, W5907 (Q50 R Carbon) is a medical device that received FDA 510(k) clearance on 2022-05-12. It is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K220740.

When was Power Wheelchair, W5907 (Q50 R Carbon) approved by the FDA?

Power Wheelchair, W5907 (Q50 R Carbon) received FDA 510(k) clearance on 2022-05-12, under approval number K220740.

What company makes Power Wheelchair, W5907 (Q50 R Carbon)?

Power Wheelchair, W5907 (Q50 R Carbon) is manufactured by Zhejiang Innuovo Rehabilitation Devices Co.,Ltd.

What is the FDA product code for Power Wheelchair, W5907 (Q50 R Carbon)?

The FDA product code for Power Wheelchair, W5907 (Q50 R Carbon) is ITI.

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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.