Cleared Traditional

K802678 - TRANSCUTANEOUS ELECTRIC NERVE STIMULATOR

K802678 is the FDA 510(k) clearance for TRANSCUTANEOUS ELECTRIC NERVE STIMULATOR by General Medical Industries, Inc.. It is a Class 2 Neurology device (product code GZJ) cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K802678 · General Medical Industries, Inc. · Neurology device
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Dec 1980
Decision
42d
Days
Class 2
Risk

K802678 is an FDA 510(k) clearance for the TRANSCUTANEOUS ELECTRIC NERVE STIMULATOR. Classified as Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ), Class II - Special Controls.

Submitted by General Medical Industries, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 10, 1980 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5890 - 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 General Medical Industries, Inc. devices

Submission Details

510(k) Number K802678 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 29, 1980
Decision Date December 10, 1980
Days to Decision 42 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
106d faster than avg
Panel avg: 148d · This submission: 42d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5890
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 - GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

All 140
Devices cleared under the same product code (GZJ) and FDA review panel - the closest regulatory comparables to K802678.
TRANSCUTANEOUS ELEC. NERVE STIMULATOR
K813501 · Empi · Dec 1981
NEUROMED SELECTRA #7720
K812704 · Medtronic Vascular · Oct 1981
NEUROPAC ULTRA I
K810593 · Medical Devices, Inc. · Mar 1981
TENSMATE EMPIMODEL 9980
K802507 · Empi · Dec 1980
EMPI MODEL 910S, TENS
K801112 · Empi · May 1980
TENZCARE DUAL-CHANNEL STIMULATOR
K800758 · 3M Company · Apr 1980