Cleared Traditional

K050290 - LERADO, COSCO

K050290 is an FDA 510(k) clearance for LERADO, manufactured by Lerado Oversea Ltd. Twn Branch (Bvi). The device is a Class 1 Physical Medicine device with product code IOR cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K050290 · Lerado Oversea Ltd. Twn Branch (Bvi) · Physical Medicine device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Feb 2005
Decision
11d
Days
Class 1
Risk

K050290 is an FDA 510(k) clearance for the LERADO, COSCO. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Lerado Oversea Ltd. Twn Branch (Bvi) (Hsin-Chu City, TW). The FDA issued a Cleared decision on February 18, 2005 after a review of 11 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.

FDA 510(k) Submission Details - K050290

510(k) Number K050290 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 07, 2005
Decision Date February 18, 2005
Days to Decision 11 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
105d faster than avg
Panel avg: 116d · This submission: 11d
Pathway characteristics
Predicate-based equivalence.

IOR Device Classification - Class 1, General Controls

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 452
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K050290.
RUNABOUT WHEELCHAIR
K050280 · Access Point Medical, LLC · Apr 2005
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CIE FOLDAWAY WHEELCHAIR
K050345 · Carlsbad International Export, Inc. · Mar 2005
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K043332 · Cycling and Health Tech. Industry R&D Center · Dec 2004
TAIWAN KING STRONG TC 04 MECHANICALWHEELCHAIR
K042652 · Taiwan King Strong Co., Ltd. · Nov 2004
LITESTREAM 500E
K042444 · Pride Mobility Products Corp. · Oct 2004
K050290 · LERADO, COSCO
Download PDF FDA Summary Lerado Oversea Ltd. T…