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FDA 510(k)

Electric Scooter

K-Number: K212090 · 2022-04-22

Decision Date2022-04-22
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Scooter is a medical device manufactured by Anhui Jbh Medical Apparatus Co., Ltd.. It received FDA 510(k) clearance on 2022-04-22 under approval number K212090. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electric Scooter?

Electric Scooter is a medical device that received FDA 510(k) clearance on 2022-04-22. It is manufactured by Anhui Jbh Medical Apparatus Co., Ltd.. The 510(k) number is K212090.

When was Electric Scooter approved by the FDA?

Electric Scooter received FDA 510(k) clearance on 2022-04-22, under approval number K212090.

What company makes Electric Scooter?

Electric Scooter is manufactured by Anhui Jbh Medical Apparatus Co., Ltd..

What is the FDA product code for Electric Scooter?

The FDA product code for Electric Scooter is INI.

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

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Related Devices (Code: INI)

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.