LUMINEX LX 100/200 INSTRUMENT— 510(k) K073506

Substantially Equivalent

Luminex Corp.

FDA 510(k) clearance K073506 for LUMINEX LX 100/200 INSTRUMENT, Substantially Equivalent on 2008-03-07. Applicant: Luminex Corp.. Device class: 2.

Clearance details

Applicant: Luminex Corp.
Product code: Code NSU
Device class: Class 2
Regulation: 21 CFR 862.2570
Advisory panel: Clinical Chemistry
Date received: 2007-12-13
Decision date: 2008-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toronto, CA

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.