IMMULITE BETA-2-MICROGLOBULIN— 510(k) K931702

Name: FDA 510(k) clearance K931702
Creator: U.S. Food and Drug Administration
Published: 1993-09-24

Substantially Equivalent

Diagnostic Products Corp.

FDA 510(k) clearance K931702 for IMMULITE BETA-2-MICROGLOBULIN, Substantially Equivalent on 1993-09-24. Applicant: Diagnostic Products Corp.. Device class: 2.

Clearance details

Applicant: Diagnostic Products Corp.
Product code: Code JZG
Device class: Class 2
Regulation: 21 CFR 866.5630
Advisory panel: Immunology
Date received: 1993-04-06
Decision date: 1993-09-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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.