FIAX TRANSFERRIN TEST KIT— 510(k) K842071

Name: FDA 510(k) clearance K842071
Creator: U.S. Food and Drug Administration
Published: 1984-07-11

Substantially Equivalent

Intl. Diagnostic Technology

FDA 510(k) clearance K842071 for FIAX TRANSFERRIN TEST KIT, Substantially Equivalent on 1984-07-11. Applicant: Intl. Diagnostic Technology. Device class: 2.

Clearance details

Applicant: Intl. Diagnostic Technology
Product code: Code DDI
Device class: Class 2
Regulation: 21 CFR 866.5880
Advisory panel: Immunology
Date received: 1984-05-23
Decision date: 1984-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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