Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F)
K-Number: K240329 · 2024-03-25
Device Summary
Frequently Asked Questions
What is the Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F)?
Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F) is a medical device that received FDA 510(k) clearance on 2024-03-25. It is manufactured by Yongkang Youha Electric Appliance Co., Ltd.. The 510(k) number is K240329.
When was Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F) approved by the FDA?
Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F) received FDA 510(k) clearance on 2024-03-25, under approval number K240329.
What company makes Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F)?
Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F) is manufactured by Yongkang Youha Electric Appliance Co., Ltd..
What is the FDA product code for Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F)?
The FDA product code for Electric wheelchair (YHW001-C;YHW001-D;YHW001-E;YHW001-F) is ITI.
Other Devices by Yongkang Youha Electric Appliance Co., Ltd.
Related Devices (Code: ITI)
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.