Cleared Traditional

ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC (K850388) - FDA 510(k) Clearance

K850388 · Instrument Technology, Inc. · Physical Medicine device
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Apr 1985
Decision
83d
Days
-
Risk

K850388 is an FDA 510(k) clearance for the ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC.

Submitted by Instrument Technology, Inc. (Mountain View, US). The FDA issued a Cleared decision on April 25, 1985 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel. 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 Instrument Technology, Inc. devices

Submission Details

510(k) Number K850388 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 1985
Decision Date April 25, 1985
Days to Decision 83 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
32d faster than avg
Panel avg: 115d · This submission: 83d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -