Mobility Scooter (X-12, X-14, X-17)
K-Number: K260237 · 2026-04-22
Decision Date2026-04-22
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Mobility Scooter (X-12, X-14, X-17) is a medical device manufactured by Wuyi Aichi Industry and Trade Co., Ltd.. It received FDA 510(k) clearance on 2026-04-22 under approval number K260237. 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 Mobility Scooter (X-12, X-14, X-17)?
Mobility Scooter (X-12, X-14, X-17) is a medical device that received FDA 510(k) clearance on 2026-04-22. It is manufactured by Wuyi Aichi Industry and Trade Co., Ltd.. The 510(k) number is K260237.
When was Mobility Scooter (X-12, X-14, X-17) approved by the FDA?
Mobility Scooter (X-12, X-14, X-17) received FDA 510(k) clearance on 2026-04-22, under approval number K260237.
What company makes Mobility Scooter (X-12, X-14, X-17)?
Mobility Scooter (X-12, X-14, X-17) is manufactured by Wuyi Aichi Industry and Trade Co., Ltd..
What is the FDA product code for Mobility Scooter (X-12, X-14, X-17)?
The FDA product code for Mobility Scooter (X-12, X-14, X-17) is INI.
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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.