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FDA 510(k)

Merlexi Craft Bariatric series of manual wheelchairs

K-Number: K240120 · 2024-07-05

ApplicantTurbo Wheelchair Co., Inc.
Decision Date2024-07-05
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Merlexi Craft Bariatric series of manual wheelchairs is a medical device manufactured by Turbo Wheelchair Co., Inc.. It received FDA 510(k) clearance on 2024-07-05 under approval number K240120. 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 Merlexi Craft Bariatric series of manual wheelchairs?

Merlexi Craft Bariatric series of manual wheelchairs is a medical device that received FDA 510(k) clearance on 2024-07-05. It is manufactured by Turbo Wheelchair Co., Inc.. The 510(k) number is K240120.

When was Merlexi Craft Bariatric series of manual wheelchairs approved by the FDA?

Merlexi Craft Bariatric series of manual wheelchairs received FDA 510(k) clearance on 2024-07-05, under approval number K240120.

What company makes Merlexi Craft Bariatric series of manual wheelchairs?

Merlexi Craft Bariatric series of manual wheelchairs is manufactured by Turbo Wheelchair Co., Inc..

What is the FDA product code for Merlexi Craft Bariatric series of manual wheelchairs?

The FDA product code for Merlexi Craft Bariatric series of manual wheelchairs is IOR.

Related Clinical Trials

NCT04668326 Mobile Manual Standing Wheelchair for SCI COMPLETED

Related PubMed Literature

PMID: 40006413 Data Reconstruction Methods in Multi-Feature Fusion CNN Model for Enhanced Human Activity Recognition. Sensors (Basel, Switzerland) (2025)

Related Devices (Code: IOR)

K162696Kuschall Advance Manual WheelchairInvacare Corporation K162686Kuschall Champion Manual WheelchairInvacare Corporation K162692Kuschall K-Series Attract Manual WheelchairInvacare Corporation K161425APEX Manual WheelchairMotion Composites K153328SUNCO Mechanical Wheelchair, model SKW-9003Danyang Sunco Machinery Co., Ltd. K151492KuduR82 A/S

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.

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