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FDA 510(k)

Electric Wheelchair (JLE-W01A-2023)

K-Number: K240255 · 2024-08-07

ApplicantZhejiang Jianrui Technology Company Limited
Decision Date2024-08-07
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Wheelchair (JLE-W01A-2023) is a medical device manufactured by Zhejiang Jianrui Technology Company Limited. It received FDA 510(k) clearance on 2024-08-07 under approval number K240255. 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 Electric Wheelchair (JLE-W01A-2023)?

Electric Wheelchair (JLE-W01A-2023) is a medical device that received FDA 510(k) clearance on 2024-08-07. It is manufactured by Zhejiang Jianrui Technology Company Limited. The 510(k) number is K240255.

When was Electric Wheelchair (JLE-W01A-2023) approved by the FDA?

Electric Wheelchair (JLE-W01A-2023) received FDA 510(k) clearance on 2024-08-07, under approval number K240255.

What company makes Electric Wheelchair (JLE-W01A-2023)?

Electric Wheelchair (JLE-W01A-2023) is manufactured by Zhejiang Jianrui Technology Company Limited.

What is the FDA product code for Electric Wheelchair (JLE-W01A-2023)?

The FDA product code for Electric Wheelchair (JLE-W01A-2023) 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.

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