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FDA 510(k)

Electric Wheelchair

K-Number: K223393 · 2023-03-16

ApplicantShanghai Bangbang Robotics Co., Ltd.
Decision Date2023-03-16
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Wheelchair is a medical device manufactured by Shanghai Bangbang Robotics Co., Ltd.. It received FDA 510(k) clearance on 2023-03-16 under approval number K223393. 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?

Electric Wheelchair is a medical device that received FDA 510(k) clearance on 2023-03-16. It is manufactured by Shanghai Bangbang Robotics Co., Ltd.. The 510(k) number is K223393.

When was Electric Wheelchair approved by the FDA?

Electric Wheelchair received FDA 510(k) clearance on 2023-03-16, under approval number K223393.

What company makes Electric Wheelchair?

Electric Wheelchair is manufactured by Shanghai Bangbang Robotics Co., Ltd..

What is the FDA product code for Electric Wheelchair?

The FDA product code for Electric Wheelchair is ITI.

Other Devices by Shanghai Bangbang Robotics Co., Ltd.

K231868Electric Wheelchair (Robooter E40), Model name: BBR-E40-01 K240339Electric Wheelchair (Robooter E60) (BBR-E60-01); Electric Wheelchair (Robooter E60) (BBR-E60-02); Electric Wheelchair (Robooter E60) (BBR-E60-03); Electric Wheelchair (Robooter E60) (BBR-E60-04); Electric Wheelchair (Robooter E60) (BBR-E60-05); Electric Wheelchair (Robooter E60) (BBR-E60-06); Electric Wheelchair (Robooter E60) (BBR-E60-07); Electric Wheelchair (Robooter E60) (BBR-E60-08) K253276Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair (Robooter E80) (BBR-E80-02)

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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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