Cleared Special

K122944 - GEMORE TRUE SINE INTERFERENTIAL STIMULATOR

K122944 is an FDA 510(k) clearance for GEMORE TRUE SINE INTERFERENTIAL STIMULATOR, manufactured by Gemore Technology Co, Ltd.. The device is a Class 2 Neurology device with product code LIH cleared through the Special 510(k) pathway after a 88-day FDA review.

K122944 · Gemore Technology Co, Ltd. · Neurology device
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Dec 2012
Decision
88d
Days
Class 2
Risk

K122944 is an FDA 510(k) clearance for the GEMORE TRUE SINE INTERFERENTIAL STIMULATOR. Classified as Interferential Current Therapy (product code LIH), Class II - Special Controls.

Submitted by Gemore Technology Co, Ltd. (Tan Shui, New Taipei City, TW). The FDA issued a Cleared decision on December 21, 2012 after a review of 88 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 Gemore Technology Co, Ltd. devices

FDA 510(k) Submission Details - K122944

510(k) Number K122944 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 24, 2012
Decision Date December 21, 2012
Days to Decision 88 days
Submission Type Special
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
60d faster than avg
Panel avg: 148d · This submission: 88d
Pathway characteristics
Modification to existing cleared device.

LIH Device Classification - Class 2, Special Controls

Product Code LIH Interferential Current Therapy
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 - LIH Interferential Current Therapy

All 41
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