Cleared Abbreviated

VECTTOR VT-200

K121662 · Alan Neuromedical Technologies, LLC · Neurology
Nov 2012
Decision
169d
Days
Class 2
Risk

About This 510(k) Submission

K121662 is an FDA 510(k) clearance for the VECTTOR VT-200, a Interferential Current Therapy (Class II — Special Controls, product code LIH), submitted by Alan Neuromedical Technologies, LLC (Corpus Christi, US). The FDA issued a Cleared decision on November 21, 2012, 169 days after receiving the submission on June 5, 2012. This device falls under the Neurology review panel. Regulated under 21 CFR 882.5890.

Submission Details

510(k) Number K121662 FDA.gov
FDA Decision Cleared SESE
Date Received June 05, 2012
Decision Date November 21, 2012
Days to Decision 169 days
Submission Type Abbreviated
Review Panel Neurology (NE)
Summary Summary PDF

Device Classification

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