FIAX TEST KIT FOR ANTI-TOXOPLASMA ANTIBO— 510(k) K790464

Name: FDA 510(k) clearance K790464
Creator: U.S. Food and Drug Administration
Published: 1979-06-13

Substantially Equivalent

Intl. Diagnostic Technology

FDA 510(k) clearance K790464 for FIAX TEST KIT FOR ANTI-TOXOPLASMA ANTIBO, Substantially Equivalent on 1979-06-13. Applicant: Intl. Diagnostic Technology. Device class: 2.

Clearance details

Applicant: Intl. Diagnostic Technology
Product code: Code GLZ
Device class: Class 2
Regulation: 21 CFR 866.3780
Advisory panel: Microbiology
Date received: 1979-03-05
Decision date: 1979-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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