Electric Wheelchair (Model: S7110)
K-Number: K200978 · 2021-04-16
Decision Date2021-04-16
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric Wheelchair (Model: S7110) is a medical device manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2021-04-16 under approval number K200978. 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: S7110)?
Electric Wheelchair (Model: S7110) is a medical device that received FDA 510(k) clearance on 2021-04-16. It is manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K200978.
When was Electric Wheelchair (Model: S7110) approved by the FDA?
Electric Wheelchair (Model: S7110) received FDA 510(k) clearance on 2021-04-16, under approval number K200978.
What company makes Electric Wheelchair (Model: S7110)?
Electric Wheelchair (Model: S7110) is manufactured by Dongguan Prestige Sporting Goods Co., Ltd..
What is the FDA product code for Electric Wheelchair (Model: S7110)?
The FDA product code for Electric Wheelchair (Model: S7110) 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.