Manual Wheelchair
K-Number: K241460 · 2024-07-11
ApplicantLichtmega Technology Co., Ltd.
Decision Date2024-07-11
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Manual Wheelchair is a medical device manufactured by Lichtmega Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-07-11 under approval number K241460. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Manual Wheelchair?
Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2024-07-11. It is manufactured by Lichtmega Technology Co., Ltd.. The 510(k) number is K241460.
When was Manual Wheelchair approved by the FDA?
Manual Wheelchair received FDA 510(k) clearance on 2024-07-11, under approval number K241460.
What company makes Manual Wheelchair?
Manual Wheelchair is manufactured by Lichtmega Technology Co., Ltd..
What is the FDA product code for Manual Wheelchair?
The FDA product code for Manual Wheelchair is IOR.
Related Clinical Trials
Other Devices by Lichtmega Technology 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.