Electric Wheelchair (KR8803)
K-Number: K241588 · 2024-11-25
Decision Date2024-11-25
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric Wheelchair (KR8803) is a medical device manufactured by Zhejiang Kairui Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2024-11-25 under approval number K241588. 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 (KR8803)?
Electric Wheelchair (KR8803) is a medical device that received FDA 510(k) clearance on 2024-11-25. It is manufactured by Zhejiang Kairui Medical Device Co., Ltd.. The 510(k) number is K241588.
When was Electric Wheelchair (KR8803) approved by the FDA?
Electric Wheelchair (KR8803) received FDA 510(k) clearance on 2024-11-25, under approval number K241588.
What company makes Electric Wheelchair (KR8803)?
Electric Wheelchair (KR8803) is manufactured by Zhejiang Kairui Medical Device Co., Ltd..
What is the FDA product code for Electric Wheelchair (KR8803)?
The FDA product code for Electric Wheelchair (KR8803) is ITI.
Other Devices by Zhejiang Kairui Medical Device 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.