Cleared Abbreviated

K080914 - ULTRASHARP CONCENTRIC NEEDLES

K080914 is an FDA 510(k) clearance for ULTRASHARP CONCENTRIC NEEDLES, manufactured by Rochester Electro Medical, Inc.. The device is a Class 2 Neurology device with product code IKT cleared through the Abbreviated 510(k) pathway after a 105-day FDA review.

K080914 · Rochester Electro Medical, Inc. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2008
Decision
105d
Days
Class 2
Risk

K080914 is an FDA 510(k) clearance for the ULTRASHARP CONCENTRIC NEEDLES. Classified as Electrode, Needle, Diagnostic Electromyograph (product code IKT), Class II - Special Controls.

Submitted by Rochester Electro Medical, Inc. (Lutz, US). The FDA issued a Cleared decision on July 15, 2008 after a review of 105 days - within the typical 510(k) review window.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 890.1385 - the FDA neurology device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Rochester Electro Medical, Inc. devices

FDA 510(k) Submission Details - K080914

510(k) Number K080914 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 01, 2008
Decision Date July 15, 2008
Days to Decision 105 days
Submission Type Abbreviated
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 148d · This submission: 105d
Pathway characteristics
Standards-based clearance path.

IKT Device Classification - Class 2, Special Controls

Product Code IKT Electrode, Needle, Diagnostic Electromyograph
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.1385
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 - IKT Electrode, Needle, Diagnostic Electromyograph

All 21
Devices cleared under the same product code (IKT) and FDA review panel - the closest regulatory comparables to K080914.
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FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550, 221-24-550
K982950 · Chalgren Enterprises, Inc. · Jun 1999
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K960591 · Chalgren Enterprises, Inc. · Jun 1996