Electric Scooter (Model: M2020)
K-Number: K230001 · 2023-07-05
Decision Date2023-07-05
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric Scooter (Model: M2020) is a medical device manufactured by Guangdong Prestige Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-07-05 under approval number K230001. 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 (Model: M2020)?
Electric Scooter (Model: M2020) is a medical device that received FDA 510(k) clearance on 2023-07-05. It is manufactured by Guangdong Prestige Technology Co., Ltd.. The 510(k) number is K230001.
When was Electric Scooter (Model: M2020) approved by the FDA?
Electric Scooter (Model: M2020) received FDA 510(k) clearance on 2023-07-05, under approval number K230001.
What company makes Electric Scooter (Model: M2020)?
Electric Scooter (Model: M2020) is manufactured by Guangdong Prestige Technology Co., Ltd..
What is the FDA product code for Electric Scooter (Model: M2020)?
The FDA product code for Electric Scooter (Model: M2020) is INI.
Related Clinical Trials
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.