Electric wheelchair (W3902)
K-Number: K241723 · 2024-09-05
Decision Date2024-09-05
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Electric wheelchair (W3902) is a medical device manufactured by Zhejiang Richall Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-09-05 under approval number K241723. 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 (W3902)?
Electric wheelchair (W3902) is a medical device that received FDA 510(k) clearance on 2024-09-05. It is manufactured by Zhejiang Richall Medical Technology Co., Ltd.. The 510(k) number is K241723.
When was Electric wheelchair (W3902) approved by the FDA?
Electric wheelchair (W3902) received FDA 510(k) clearance on 2024-09-05, under approval number K241723.
What company makes Electric wheelchair (W3902)?
Electric wheelchair (W3902) is manufactured by Zhejiang Richall Medical Technology Co., Ltd..
What is the FDA product code for Electric wheelchair (W3902)?
The FDA product code for Electric wheelchair (W3902) is ITI.
Other Devices by Zhejiang Richall Medical Technology 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.