Cleared Traditional

K881464 - MULTIMODE(TM) INTERFACE SYS. FOR EVEREST & JENNING

K881464 is an FDA 510(k) clearance for MULTIMODE(TM) INTERFACE SYS. FOR EVERES..., manufactured by Dufco Electronics, Inc.. The device is a Class 2 Physical Medicine device with product code ITI cleared through the Traditional 510(k) pathway after a 102-day FDA review.

K881464 · Dufco Electronics, Inc. · Physical Medicine device
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Jul 1988
Decision
102d
Days
Class 2
Risk

K881464 is an FDA 510(k) clearance for the MULTIMODE(TM) INTERFACE SYS. FOR EVEREST & JENNING. Classified as Wheelchair, Powered (product code ITI), Class II - Special Controls.

Submitted by Dufco Electronics, Inc. (Cambria, US). The FDA issued a Cleared decision on July 18, 1988 after a review of 102 days - within the typical 510(k) review window.

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: 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 Dufco Electronics, Inc. devices

FDA 510(k) Submission Details - K881464

510(k) Number K881464 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1988
Decision Date July 18, 1988
Days to Decision 102 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
13d faster than avg
Panel avg: 115d · This submission: 102d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ITI Device Classification - Class 2, Special Controls

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 406
Devices cleared under the same product code (ITI) and FDA review panel - the closest regulatory comparables to K881464.
MODEL #1556 HEAVY-DUTY JOYSTICK
K880365 · Invacare Corp. · Sep 1988
CLIPPER POWER DRIVE WHEELCHAIR
K883339 · Everest & Jennings, Inc. · Aug 1988
TASH PILOT SYSTEM
K874417 · Everest & Jennings, Inc. · Aug 1988
HOT WHEELS
K873895 · Everest & Jennings, Inc. · Nov 1987
POIRIER POWERED WHEELCHAIR
K864791 · Roseburg SA · Feb 1987
CHILD'S ROLLS POWERED WHEELCHAIR
K863250 · Invacare Corp. · Aug 1986