Cleared Traditional

K934560 - WIZARD PEDIATRIC WHEELCHAIR

K934560 is an FDA 510(k) clearance for WIZARD PEDIATRIC WHEELCHAIR, manufactured by Snug Seat, Inc.. The device is a Class 1 Physical Medicine device with product code IOR cleared through the Traditional 510(k) pathway after a 108-day FDA review.

K934560 · Snug Seat, Inc. · Physical Medicine device
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Jan 1994
Decision
108d
Days
Class 1
Risk

K934560 is an FDA 510(k) clearance for the WIZARD PEDIATRIC WHEELCHAIR. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Snug Seat, Inc. (Matthews, US). The FDA issued a Cleared decision on January 7, 1994 after a review of 108 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Snug Seat, Inc. devices

FDA 510(k) Submission Details - K934560

510(k) Number K934560 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 21, 1993
Decision Date January 07, 1994
Days to Decision 108 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
7d faster than avg
Panel avg: 115d · This submission: 108d
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 141
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K934560.
TRACER SERIES MANUAL WHEELCHAIRS
K935398 · Invacare Corp. · Mar 1994
RECORD
K940303 · Everest & Jennings, Inc. · Feb 1994
NITRO
K940304 · Everest & Jennings, Inc. · Feb 1994
ACTION WIZARD PEDIATRIC MANUAL WHEELCHAIR
K934646 · Invacare Corp. · Dec 1993
UNIVERSAL WHEELCHAIR
K930411 · Everest & Jennings, Inc. · Mar 1993
PREMIER 2 WHEELCHAIR
K930412 · Everest & Jennings, Inc. · Mar 1993