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FDA 510(k)

Electric Wheelchair (F309)

K-Number: K250758 · 2025-05-09

ApplicantChangshu Pingfang Wheelchair Co., Ltd.
Decision Date2025-05-09
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Wheelchair (F309) is a medical device manufactured by Changshu Pingfang Wheelchair Co., Ltd.. It received FDA 510(k) clearance on 2025-05-09 under approval number K250758. 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 (F309)?

Electric Wheelchair (F309) is a medical device that received FDA 510(k) clearance on 2025-05-09. It is manufactured by Changshu Pingfang Wheelchair Co., Ltd.. The 510(k) number is K250758.

When was Electric Wheelchair (F309) approved by the FDA?

Electric Wheelchair (F309) received FDA 510(k) clearance on 2025-05-09, under approval number K250758.

What company makes Electric Wheelchair (F309)?

Electric Wheelchair (F309) is manufactured by Changshu Pingfang Wheelchair Co., Ltd..

What is the FDA product code for Electric Wheelchair (F309)?

The FDA product code for Electric Wheelchair (F309) is ITI.

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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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