Electric Scooter (M2085, S2091)
K-Number: K240272 · 2024-07-16
Decision Date2024-07-16
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric Scooter (M2085, S2091) is a medical device manufactured by Guangdong Prestige Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-07-16 under approval number K240272. 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 (M2085, S2091)?
Electric Scooter (M2085, S2091) is a medical device that received FDA 510(k) clearance on 2024-07-16. It is manufactured by Guangdong Prestige Technology Co., Ltd.. The 510(k) number is K240272.
When was Electric Scooter (M2085, S2091) approved by the FDA?
Electric Scooter (M2085, S2091) received FDA 510(k) clearance on 2024-07-16, under approval number K240272.
What company makes Electric Scooter (M2085, S2091)?
Electric Scooter (M2085, S2091) is manufactured by Guangdong Prestige Technology Co., Ltd..
What is the FDA product code for Electric Scooter (M2085, S2091)?
The FDA product code for Electric Scooter (M2085, S2091) is INI.
Other Devices by Guangdong Prestige 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.