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FDA 510(k)

Electric wheelchair (S7204/S7205)

K-Number: K202632 · 2021-04-08

ApplicantDongguan Prestige Sporting Goods Co., Ltd.
Decision Date2021-04-08
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric wheelchair (S7204/S7205) is a medical device manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2021-04-08 under approval number K202632. 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 (S7204/S7205)?

Electric wheelchair (S7204/S7205) is a medical device that received FDA 510(k) clearance on 2021-04-08. It is manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K202632.

When was Electric wheelchair (S7204/S7205) approved by the FDA?

Electric wheelchair (S7204/S7205) received FDA 510(k) clearance on 2021-04-08, under approval number K202632.

What company makes Electric wheelchair (S7204/S7205)?

Electric wheelchair (S7204/S7205) is manufactured by Dongguan Prestige Sporting Goods Co., Ltd..

What is the FDA product code for Electric wheelchair (S7204/S7205)?

The FDA product code for Electric wheelchair (S7204/S7205) is ITI.

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.

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