Electric Wheelchair (Model: S7110)
K-Number: K200978 · 2021-04-16
Device Summary
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. The listed applicant is Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K200978.
When did Electric Wheelchair (Model: S7110) receive FDA 510(k) clearance?
Electric Wheelchair (Model: S7110) received FDA 510(k) clearance on 2021-04-16, under 510(k) number K200978.
Who is the listed applicant for Electric Wheelchair (Model: S7110)?
The FDA 510(k) record lists Dongguan Prestige Sporting Goods Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electric Wheelchair (Model: S7110)?
The FDA product code for Electric Wheelchair (Model: S7110) is ITI.
Other records listing Dongguan Prestige Sporting Goods Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: ITI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.