Electric wheelchair (KR-8807)
K-Number: K242791 · 2024-11-12
Decision Date2024-11-12
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric wheelchair (KR-8807) is a medical device manufactured by Zhejiang Kairui Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2024-11-12 under approval number K242791. 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 (KR-8807)?
Electric wheelchair (KR-8807) is a medical device that received FDA 510(k) clearance on 2024-11-12. It is manufactured by Zhejiang Kairui Medical Device Co., Ltd.. The 510(k) number is K242791.
When was Electric wheelchair (KR-8807) approved by the FDA?
Electric wheelchair (KR-8807) received FDA 510(k) clearance on 2024-11-12, under approval number K242791.
What company makes Electric wheelchair (KR-8807)?
Electric wheelchair (KR-8807) is manufactured by Zhejiang Kairui Medical Device Co., Ltd..
What is the FDA product code for Electric wheelchair (KR-8807)?
The FDA product code for Electric wheelchair (KR-8807) is ITI.
Other Devices by Zhejiang Kairui Medical Device Co., Ltd.
Related Devices (Code: ITI)
K161241e-fix E35/E36Alber GmbH
K153636Liberator Powered Wheelchair with Solar CompanionSolar Mobilityllc
K160031Quickie Pulse (Models 6BC, 6SC, 6CC, 5BC, 5CC, 6MPC) and Zippie ZM-310 (Models BC, SC)Sunrise Medical (Us), LLC
K151717twionAlber GmbH
K153543WHILL Model MWhill, Inc.
K152672Cajun Commando 4x4Lil Critter, LLC
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.