Cleared Traditional

K881915 - DANTEC MAGNETIC STIMULATOR

K881915 is an FDA 510(k) clearance for DANTEC MAGNETIC STIMULATOR, manufactured by Dantec Electronics, Inc.. The device is a Class 2 Neurology device with product code GWF cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K881915 · Dantec Electronics, Inc. · Neurology device
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Oct 1988
Decision
161d
Days
Class 2
Risk

K881915 is an FDA 510(k) clearance for the DANTEC MAGNETIC STIMULATOR. Classified as Stimulator, Electrical, Evoked Response (product code GWF), Class II - Special Controls.

Submitted by Dantec Electronics, Inc. (Allendale, US). The FDA issued a Cleared decision on October 17, 1988 after a review of 161 days - an extended review cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1870 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Dantec Electronics, Inc. devices

FDA 510(k) Submission Details - K881915

510(k) Number K881915 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 09, 1988
Decision Date October 17, 1988
Days to Decision 161 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
13d slower than avg
Panel avg: 148d · This submission: 161d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GWF Device Classification - Class 2, Special Controls

Product Code GWF Stimulator, Electrical, Evoked Response
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1870
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 - GWF Stimulator, Electrical, Evoked Response

All 104
Devices cleared under the same product code (GWF) and FDA review panel - the closest regulatory comparables to K881915.
CANTATA EMG/EVOKED RESPONSE SYSTEM
K896567 · Dantec Medical, Inc. · Feb 1990
MEM-7102
K890274 · Nihon Kohden America, Inc. · May 1989
TECA/MEDELEC 'CONCEPT' P420
K884870 · Teca, Inc. · Feb 1989
CADWELL EXCEL
K880088 · Cadwell Laboratories, Inc. · May 1988
NOVAMETRIX MODEL 200 MAGSTIM
K871338 · Novametrix Medical Systems, Inc. · Aug 1987
EES 10 ELECTRODELESS ELECTRICAL STIMULATOR
K863175 · Cadwell Laboratories, Inc. · Jan 1987