Cleared Traditional

K942965 - COMPUTER DYNO/GONIO/MYO GRAPHY

K942965 is an FDA 510(k) clearance for COMPUTER DYNO/GONIO/MYO GRAPHY, manufactured by Infotronic Medical Engineering. The device is a Class 2 Neurology device with product code IKN cleared through the Traditional 510(k) pathway after a 470-day FDA review.

K942965 · Infotronic Medical Engineering · Neurology device
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Oct 1995
Decision
470d
Days
Class 2
Risk

K942965 is an FDA 510(k) clearance for the COMPUTER DYNO/GONIO/MYO GRAPHY. Classified as Electromyograph, Diagnostic (product code IKN), Class II - Special Controls.

Submitted by Infotronic Medical Engineering (Severna Park, US). The FDA issued a Cleared decision on October 7, 1995 after a review of 470 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 890.1375 - the FDA neurology 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 Neurology submissions.

View all Infotronic Medical Engineering devices

FDA 510(k) Submission Details - K942965

510(k) Number K942965 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 1994
Decision Date October 07, 1995
Days to Decision 470 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
322d slower than avg
Panel avg: 148d · This submission: 470d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IKN Device Classification - Class 2, Special Controls

Product Code IKN Electromyograph, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.1375
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 Neurology devices follow this clearance model.

Regulatory Peers - IKN Electromyograph, Diagnostic

All 43
Devices cleared under the same product code (IKN) and FDA review panel - the closest regulatory comparables to K942965.
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K893130 · Bio-Logic Systems Corp. · Mar 1990