Mobility Scooter (CL-Q3, CL-Q4)
K-Number: K253631 · 2026-02-23
Decision Date2026-02-23
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Mobility Scooter (CL-Q3, CL-Q4) is a medical device manufactured by Zhejiang Wei Ling New Energy Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-23 under approval number K253631. 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 (CL-Q3, CL-Q4)?
Mobility Scooter (CL-Q3, CL-Q4) is a medical device that received FDA 510(k) clearance on 2026-02-23. It is manufactured by Zhejiang Wei Ling New Energy Technology Co., Ltd.. The 510(k) number is K253631.
When was Mobility Scooter (CL-Q3, CL-Q4) approved by the FDA?
Mobility Scooter (CL-Q3, CL-Q4) received FDA 510(k) clearance on 2026-02-23, under approval number K253631.
What company makes Mobility Scooter (CL-Q3, CL-Q4)?
Mobility Scooter (CL-Q3, CL-Q4) is manufactured by Zhejiang Wei Ling New Energy Technology Co., Ltd..
What is the FDA product code for Mobility Scooter (CL-Q3, CL-Q4)?
The FDA product code for Mobility Scooter (CL-Q3, CL-Q4) 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.