Cleared Traditional

K123902 - PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)

K123902 is an FDA 510(k) clearance for PHYSICAL MONITORING REGISTRATION UNIT-S..., manufactured by Oktx, LLC. The device is a Class 2 Neurology device with product code IKN cleared through the Traditional 510(k) pathway after a 269-day FDA review.

K123902 · Oktx, LLC · Neurology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Sep 2013
Decision
269d
Days
Class 2
Risk

K123902 is an FDA 510(k) clearance for the PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S). Classified as Electromyograph, Diagnostic (product code IKN), Class II - Special Controls.

Submitted by Oktx, LLC (Tulsa, US). The FDA issued a Cleared decision on September 13, 2013 after a review of 269 days - an extended review cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 890.1375 - 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.

FDA 510(k) Submission Details - K123902

510(k) Number K123902 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 18, 2012
Decision Date September 13, 2013
Days to Decision 269 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
120d slower than avg
Panel avg: 149d · This submission: 269d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IKN Device Classification - Class 2, Special Controls

Product Code IKN Electromyograph, Diagnostic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.1375
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 - IKN Electromyograph, Diagnostic

All 57
Devices cleared under the same product code (IKN) and FDA review panel - the closest regulatory comparables to K123902.
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K123902 · PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)
Download PDF FDA Summary Oktx, LLC