Cleared Traditional

K842956 - NICOLET VIKING

K842956 is an FDA 510(k) clearance for NICOLET VIKING, manufactured by Nicolet Biomedical Instruments. The device is a Class 2 Neurology device with product code IKN cleared through the Traditional 510(k) pathway after a 7-day FDA review.

K842956 · Nicolet Biomedical Instruments · Neurology device
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Aug 1984
Decision
7d
Days
Class 2
Risk

K842956 is an FDA 510(k) clearance for the NICOLET VIKING. Classified as Electromyograph, Diagnostic (product code IKN), Class II - Special Controls.

Submitted by Nicolet Biomedical Instruments (Mchenry, US). The FDA issued a Cleared decision on August 3, 1984 after a review of 7 days - a notably fast clearance cycle.

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: 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 Nicolet Biomedical Instruments devices

FDA 510(k) Submission Details - K842956

510(k) Number K842956 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 27, 1984
Decision Date August 03, 1984
Days to Decision 7 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
141d faster than avg
Panel avg: 148d · This submission: 7d
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 40
Devices cleared under the same product code (IKN) and FDA review panel - the closest regulatory comparables to K842956.
EMG NAVIGATOR & EMG TRAVELER
K893130 · Bio-Logic Systems Corp. · Mar 1990
MODIFIED NICOLET VIKING SYSTEM
K880573 · Nicolet Biomedical Instruments · Mar 1988
KC/EMG DIAGNOSTIC ELECTROMYOGRAPH
K864630 · Chattanooga Group, Inc. · Dec 1986
CA2000
K842611 · Nicolet Biomedical Instruments · Jul 1984
COMPACT AUDITORY
K842612 · Nicolet Biomedical Instruments · Jul 1984
COMPACT VISUAL
K842613 · Nicolet Biomedical Instruments · Jul 1984