RADIOIMMUNOASSAY FOR TOTAL IGE HUMAN— 510(k) K840103

Name: FDA 510(k) clearance K840103
Creator: U.S. Food and Drug Administration
Published: 1984-02-10

Substantially Equivalent

Techniclone Intl.

FDA 510(k) clearance K840103 for RADIOIMMUNOASSAY FOR TOTAL IGE HUMAN, Substantially Equivalent on 1984-02-10. Applicant: Techniclone Intl.. Device class: 2.

Clearance details

Applicant: Techniclone Intl.
Product code: Code JHR
Device class: Class 2
Regulation: 21 CFR 866.5510
Advisory panel: Immunology
Date received: 1984-01-10
Decision date: 1984-02-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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