Folding Mobility Scooter (KD101)
K-Number: K252502 · 2025-10-06
Decision Date2025-10-06
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Folding Mobility Scooter (KD101) is a medical device manufactured by Nanjing Kangni Smart Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-10-06 under approval number K252502. 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 Folding Mobility Scooter (KD101)?
Folding Mobility Scooter (KD101) is a medical device that received FDA 510(k) clearance on 2025-10-06. It is manufactured by Nanjing Kangni Smart Technology Co., Ltd.. The 510(k) number is K252502.
When was Folding Mobility Scooter (KD101) approved by the FDA?
Folding Mobility Scooter (KD101) received FDA 510(k) clearance on 2025-10-06, under approval number K252502.
What company makes Folding Mobility Scooter (KD101)?
Folding Mobility Scooter (KD101) is manufactured by Nanjing Kangni Smart Technology Co., Ltd..
What is the FDA product code for Folding Mobility Scooter (KD101)?
The FDA product code for Folding Mobility Scooter (KD101) is INI.
Other Devices by Nanjing Kangni Smart Technology 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.