Electric wheelchair (Model: S7012)
K-Number: K200857 · 2020-12-17
Decision Date2020-12-17
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric wheelchair (Model: S7012) is a medical device manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2020-12-17 under approval number K200857. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Electric wheelchair (Model: S7012)?
Electric wheelchair (Model: S7012) is a medical device that received FDA 510(k) clearance on 2020-12-17. It is manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K200857.
When was Electric wheelchair (Model: S7012) approved by the FDA?
Electric wheelchair (Model: S7012) received FDA 510(k) clearance on 2020-12-17, under approval number K200857.
What company makes Electric wheelchair (Model: S7012)?
Electric wheelchair (Model: S7012) is manufactured by Dongguan Prestige Sporting Goods Co., Ltd..
What is the FDA product code for Electric wheelchair (Model: S7012)?
The FDA product code for Electric wheelchair (Model: S7012) is ITI.
Related Clinical Trials
Other Devices by Dongguan Prestige Sporting Goods 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.