Cleared Traditional

ROLL A BOUT WALKER (K941301) - FDA 510(k) Clearance

Class I Physical Medicine device.

K941301 · Roll A Bout Corp. · Physical Medicine device
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May 1994
Decision
46d
Days
Class 1
Risk

K941301 is an FDA 510(k) clearance for the ROLL A BOUT WALKER. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Roll A Bout Corp. (Dover, US). The FDA issued a Cleared decision on May 2, 1994 after a review of 46 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 Roll A Bout Corp. devices

Submission Details

510(k) Number K941301 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 17, 1994
Decision Date May 02, 1994
Days to Decision 46 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 115d · This submission: 46d
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 456
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K941301.
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