Cleared Special

K160517 - ARIES System (FDA 510(k) Clearance)

Apr 2016
Decision
48d
Days
Class 2
Risk

K160517 is an FDA 510(k) clearance for the ARIES System. This device is classified as a Real Time Nucleic Acid Amplification System (Class II - Special Controls, product code OOI).

Submitted by Luminex Corporation (Austin, US). The FDA issued a Cleared decision on April 12, 2016, 48 days after receiving the submission on February 24, 2016.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 862.2570. The System Is A Clinical Multiplex Instrument Intended To Measure And Sort Multiple Signals Generated My Multiple Probes, Intercalating Dyes, Or Other Ligands In An Assay From A Clinical Sample. Signals May Be Generated By Fluorescence Or Other Phenomena And May Be Measured Using Filters On A Photodiode Or Other Detector. It May Integrate Sample And/or Reagent Handling, Amplification, Dedicated Instrument Control, Data Acquisition Software, Raw Data Storage Mechanisms And Other Essential Hardware Components Along With The Signal Reader Unit. The System Is Used With Specific Assays To Comprise An Assay Test System..

Submission Details

510(k) Number K160517 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 24, 2016
Decision Date April 12, 2016
Days to Decision 48 days
Submission Type Special
Review Panel Microbiology (MI)
Summary Statement

Device Classification

Product Code OOI - Real Time Nucleic Acid Amplification System
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.2570
Definition The System Is A Clinical Multiplex Instrument Intended To Measure And Sort Multiple Signals Generated My Multiple Probes, Intercalating Dyes, Or Other Ligands In An Assay From A Clinical Sample. Signals May Be Generated By Fluorescence Or Other Phenomena And May Be Measured Using Filters On A Photodiode Or Other Detector. It May Integrate Sample And/or Reagent Handling, Amplification, Dedicated Instrument Control, Data Acquisition Software, Raw Data Storage Mechanisms And Other Essential Hardware Components Along With The Signal Reader Unit. The System Is Used With Specific Assays To Comprise An Assay Test System.