Cleared Traditional

K162966 - TxRx Knee 15 Flare MR Coil 1.5T (FDA 510(k) Clearance)

Nov 2016
Decision
37d
Days
Class 2
Risk

K162966 is an FDA 510(k) clearance for the TxRx Knee 15 Flare MR Coil 1.5T. This device is classified as a Coil, Magnetic Resonance, Specialty (Class II - Special Controls, product code MOS).

Submitted by Quality Electrodynamics, LLC (Mayfield Heights, US). The FDA issued a Cleared decision on November 30, 2016, 37 days after receiving the submission on October 24, 2016.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1000.

Submission Details

510(k) Number K162966 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 24, 2016
Decision Date November 30, 2016
Days to Decision 37 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code MOS — Coil, Magnetic Resonance, Specialty
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.1000

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