Cleared Special

K010782 - TRANSAMERICAN TENS

K010782 is an FDA 510(k) clearance for TRANSAMERICAN TENS, manufactured by Transamerica Medical Systems. The device is a Class 2 Neurology device with product code GZJ cleared through the Special 510(k) pathway after a 43-day FDA review.

K010782 · Transamerica Medical Systems · Neurology device
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Apr 2001
Decision
43d
Days
Class 2
Risk

K010782 is an FDA 510(k) clearance for the TRANSAMERICAN TENS. Classified as Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ), Class II - Special Controls.

Submitted by Transamerica Medical Systems (Holyoke, US). The FDA issued a Cleared decision on April 27, 2001 after a review of 43 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Transamerica Medical Systems devices

FDA 510(k) Submission Details - K010782

510(k) Number K010782 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 2001
Decision Date April 27, 2001
Days to Decision 43 days
Submission Type Special
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
105d faster than avg
Panel avg: 148d · This submission: 43d
Pathway characteristics
Modification to existing cleared device.

GZJ Device Classification - Class 2, Special Controls

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 229
Devices cleared under the same product code (GZJ) and FDA review panel - the closest regulatory comparables to K010782.
WINNER CM4 COMBINATION UNIT
K012848 · Rich-Mar Corp. · Oct 2001
MULTI-STIM, MODEL MS-100
K001897 · Metron Medical Australia, Pty, Ltd. · Jun 2001
ELECTRO-NERVE STIMULATOR TENS, MODEL HE-DIGITAL
K010209 · Biomedical Life Systems, Inc. · Jun 2001
ANALGESIC PULSER, MODEL AP-439
K993229 · Johari Electro-Tech Co. · Feb 2001
STIMATE N601 TENS
K003487 · Everyway Medical Instruments Co.,Ltd · Jan 2001
MEDISANA DIGITAL TENS
K994265 · Fuji Dynamics Limited · Jul 2000