Cleared Traditional

INTELECT IFC2

K924666 · Chattanooga Group, Inc. · Neurology
Mar 1993
Decision
170d
Days
Class 2
Risk

About This 510(k) Submission

K924666 is an FDA 510(k) clearance for the INTELECT IFC2, a Interferential Current Therapy (Class II — Special Controls, product code LIH), submitted by Chattanooga Group, Inc. (Hixson, US). The FDA issued a Cleared decision on March 5, 1993, 170 days after receiving the submission on September 16, 1992. This device falls under the Neurology review panel. Regulated under 21 CFR 882.5890.

Submission Details

510(k) Number K924666 FDA.gov
FDA Decision Cleared SESE
Date Received September 16, 1992
Decision Date March 05, 1993
Days to Decision 170 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement

Device Classification

Product Code LIH — Interferential Current Therapy
Device Class Class II — Special Controls
CFR Regulation 21 CFR 882.5890

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