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FDA 510(k)

Portable Folding Electric Wheelchair (Model: DC01)

K-Number: K212092 · 2022-05-06

ApplicantAnhui Jbh Medical Apparatus Co., Ltd.
Decision Date2022-05-06
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Portable Folding Electric Wheelchair (Model: DC01) is a medical device manufactured by Anhui Jbh Medical Apparatus Co., Ltd.. It received FDA 510(k) clearance on 2022-05-06 under approval number K212092. 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 Portable Folding Electric Wheelchair (Model: DC01)?

Portable Folding Electric Wheelchair (Model: DC01) is a medical device that received FDA 510(k) clearance on 2022-05-06. It is manufactured by Anhui Jbh Medical Apparatus Co., Ltd.. The 510(k) number is K212092.

When was Portable Folding Electric Wheelchair (Model: DC01) approved by the FDA?

Portable Folding Electric Wheelchair (Model: DC01) received FDA 510(k) clearance on 2022-05-06, under approval number K212092.

What company makes Portable Folding Electric Wheelchair (Model: DC01)?

Portable Folding Electric Wheelchair (Model: DC01) is manufactured by Anhui Jbh Medical Apparatus Co., Ltd..

What is the FDA product code for Portable Folding Electric Wheelchair (Model: DC01)?

The FDA product code for Portable Folding Electric Wheelchair (Model: DC01) is ITI.

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Other Devices by Anhui Jbh Medical Apparatus Co., Ltd.

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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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