Cleared Traditional

K030564 - THERMOSKIN CONDUCTIVE PADS

K030564 is an FDA 510(k) clearance for THERMOSKIN CONDUCTIVE PADS, manufactured by United Pacific, Inc.. The device is a Class 2 Neurology device with product code GXY cleared through the Traditional 510(k) pathway after a 203-day FDA review.

K030564 · United Pacific, Inc. · Neurology device
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Sep 2003
Decision
203d
Days
Class 2
Risk

K030564 is an FDA 510(k) clearance for the THERMOSKIN CONDUCTIVE PADS. Classified as Electrode, Cutaneous (product code GXY), Class II - Special Controls.

Submitted by United Pacific, Inc. (Columbia, US). The FDA issued a Cleared decision on September 12, 2003 after a review of 203 days - an extended review cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1320 - 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 United Pacific, Inc. devices

FDA 510(k) Submission Details - K030564

510(k) Number K030564 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 21, 2003
Decision Date September 12, 2003
Days to Decision 203 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
55d slower than avg
Panel avg: 148d · This submission: 203d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GXY Device Classification - Class 2, Special Controls

Product Code GXY Electrode, Cutaneous
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1320
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 - GXY Electrode, Cutaneous

All 275
Devices cleared under the same product code (GXY) and FDA review panel - the closest regulatory comparables to K030564.
BIS PEDIATRIC SENSOR
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