Cleared Traditional

K800758 - TENZCARE DUAL-CHANNEL STIMULATOR

K800758 is the FDA 510(k) clearance for TENZCARE DUAL-CHANNEL STIMULATOR by 3M Company. It is a Class 2 Neurology device (product code GZJ) cleared through the Traditional 510(k) pathway after a 6-day FDA review.

K800758 · 3M Company · Neurology device
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Apr 1980
Decision
6d
Days
Class 2
Risk

K800758 is an FDA 510(k) clearance for the TENZCARE DUAL-CHANNEL STIMULATOR. Classified as Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ), Class II - Special Controls.

Submitted by 3M Company (White City, US). The FDA issued a Cleared decision on April 10, 1980 after a review of 6 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 3M Company devices

Submission Details

510(k) Number K800758 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 04, 1980
Decision Date April 10, 1980
Days to Decision 6 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
142d faster than avg
Panel avg: 148d · This submission: 6d
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 116
Devices cleared under the same product code (GZJ) and FDA review panel - the closest regulatory comparables to K800758.
NEUROPAC ULTRA I
K810593 · Medical Devices, Inc. · Mar 1981
TENSMATE EMPIMODEL 9980
K802507 · Empi · Dec 1980
EMPI MODEL 910S, TENS
K801112 · Empi · May 1980
MODEL 980D TENS NEUROPACER
K792522 · Empi · Dec 1979
MEDTRONIC MODEL 7728 NEUROMOD
K792311 · Medtronic Vascular · Nov 1979
STIMULATOR, MENTOR 100 NERVE
K790011 · Mentor Corp. · Mar 1979