Cleared Traditional

K930413 - PREMIER CLASSIC

K930413 is the FDA 510(k) clearance for PREMIER CLASSIC by Everest & Jennings, Inc.. It is a Class 1 Physical Medicine device (product code IOR) cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K930413 · Everest & Jennings, Inc. · Physical Medicine device
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Mar 1993
Decision
64d
Days
Class 1
Risk

K930413 is an FDA 510(k) clearance for the PREMIER CLASSIC. Classified as Wheelchair, Mechanical (product code IOR), Class I - General Controls.

Submitted by Everest & Jennings, Inc. (Earth City, US). The FDA issued a Cleared decision on March 31, 1993 after a review of 64 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 Everest & Jennings, Inc. devices

Submission Details

510(k) Number K930413 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 26, 1993
Decision Date March 31, 1993
Days to Decision 64 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
51d faster than avg
Panel avg: 115d · This submission: 64d
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 77
Devices cleared under the same product code (IOR) and FDA review panel - the closest regulatory comparables to K930413.
ACTION PATRIOT MANUAL WHEELCHAIR
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TRACER SERIES MANUAL WHEELCHAIRS
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ACTION WIZARD PEDIATRIC MANUAL WHEELCHAIR
K934646 · Invacare Corp. · Dec 1993
ACTION FX MANUAL WHEELCHAIR
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VOYAGEUR AND LAURENTIAN SERIES WHEELCHAIR
K920391 · Invacare Corp. · Feb 1992
ACTION SERIES MANUAL WHEELCHAIRS, VARIOUS MODELS
K914553 · Invacare Corp. · Oct 1991