Cleared Traditional

Manual Wheelchair (K241460) - FDA 510(k) Clearance

Class I Physical Medicine device.

K241460 · Lichtmega Technology Co., Ltd. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2024
Decision
49d
Days
Class 1
Risk

K241460 is an FDA 510(k) clearance for the Manual Wheelchair. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Lichtmega Technology Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on July 11, 2024 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3850 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Lichtmega Technology Co., Ltd. devices

Submission Details

510(k) Number K241460 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 23, 2024
Decision Date July 11, 2024
Days to Decision 49 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 115d · This submission: 49d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code IOR Wheelchair, Mechanical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3850
Definition A Mechanical Wheelchair Is A Manually Operated Device With Wheels That Is Intended For Medical Purposes To Provide Mobility To Persons Restricted To A Sitting Position. Fda Interprets “mobility To Persons Restricted To A Sitting Position” To Mean The Device Type Is Intended To Provide Mobility To Individuals Who Have Mobility Impairments And/or Require An Assistive Device For Mobility.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IOR Wheelchair, Mechanical

All 52
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K241460.
Bowhead ERA Wheelchairs
K243111 · Bowhead Design Corp. · Jan 2025
Manual Wheelchair (MASY23)
K242722 · Sichuan Ast Medical Equipment Co., Ltd. · Nov 2024
Manual Wheelchair (SYIV100-CA9221)
K242560 · Foshan Shunkangda Medical Tech Co., Ltd. · Oct 2024
Merlexi Craft Bariatric series of manual wheelchairs
K240120 · Turbo Wheelchair Co., Inc. · Jul 2024
YJ-K1/K2 Wheelchair (YJ-K1F 16 NDE
K232230 · Zhenjiang Assure Medical Equipment Co., Ltd. · Oct 2023
Reclining wheelchair (YJ-011S 16”D, YJ-011S 16”DF, YJ-011S 18”D, YJ-011S 18”DF, YJ-011S 20”D, YJ-011S 20”DF)
K232198 · Zhenjiang Assure Medical Equipment Co., Ltd. · Sep 2023