LIAISON ALDOSTERONE, LIAISON ALDOSTERONE CONTROL SET, LIAISON ALDOSTERONE CALIBRATION VERIFIERS— 510(k) K130321

Name: FDA 510(k) clearance K130321
Creator: U.S. Food and Drug Administration
Published: 2013-04-09

Substantially Equivalent

Diasorin

FDA 510(k) clearance K130321 for LIAISON ALDOSTERONE, LIAISON ALDOSTERONE CONTROL SET, LIAISON ALDOSTERONE CALIBRATION VERIFIERS, Substantially Equivalent on 2013-04-09. Applicant: Diasorin. Device class: 2.

Clearance details

Applicant: Diasorin
Product code: Code CJM
Device class: Class 2
Regulation: 21 CFR 862.1045
Advisory panel: Clinical Chemistry
Date received: 2013-02-08
Decision date: 2013-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stillwater, MN, US

Download summary PDF View on FDA.gov ↗

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