Cleared Traditional

K925865 - KID POWER

K925865 is the FDA 510(k) clearance for KID POWER by Everest & Jennings, Inc.. It is a Class 2 Physical Medicine device (product code ITI) cleared through the Traditional 510(k) pathway after a 494-day FDA review.

K925865 · Everest & Jennings, Inc. · Physical Medicine device
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Mar 1994
Decision
494d
Days
Class 2
Risk

K925865 is an FDA 510(k) clearance for the KID POWER. Classified as Wheelchair, Powered (product code ITI), Class II - Special Controls.

Submitted by Everest & Jennings, Inc. (Earth City, US). The FDA issued a Cleared decision on March 28, 1994 after a review of 494 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3860 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Physical Medicine submissions.

View all Everest & Jennings, Inc. devices

Submission Details

510(k) Number K925865 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 19, 1992
Decision Date March 28, 1994
Days to Decision 494 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
379d slower than avg
Panel avg: 115d · This submission: 494d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code ITI Wheelchair, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.3860
Definition A Powered Wheelchair Is A Battery-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 Require An Assistive Device For Mobility. Note: This Type Of Device Is Not Intended To Climb Stairs (see Product Code: Imk).
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Physical Medicine devices follow this clearance model.

Regulatory Peers - ITI Wheelchair, Powered

All 171
Devices cleared under the same product code (ITI) and FDA review panel - the closest regulatory comparables to K925865.
ACTION STORM RANGER II, ACTION STORM POWER 9000
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MODEL MCC - MKIV MICRO COMPUTER CONTROLS
K940972 · Invacare Corp. · Jun 1994
ACTION STORM POWER WHEELCHAIR
K940051 · Invacare Corp. · Mar 1994
ACTION TIGER POWERED WHEELCHAIR
K930676 · Invacare Corp. · Mar 1994
MICRO COMPUTER CONTROLS, MODEL# MCC-MK-RII-X
K914938 · Invacare Corp. · Jan 1992