MEDIX BIOTECH FERRITIN ENZYME IMMUNOASSAY TEST KIT— 510(k) K873730

Name: FDA 510(k) clearance K873730
Creator: U.S. Food and Drug Administration
Published: 1987-11-04

Substantially Equivalent

Medix Biotech, Inc.

FDA 510(k) clearance K873730 for MEDIX BIOTECH FERRITIN ENZYME IMMUNOASSAY TEST KIT, Substantially Equivalent on 1987-11-04. Applicant: Medix Biotech, Inc.. Device class: 2.

Clearance details

Applicant: Medix Biotech, Inc.
Product code: Code JMG
Device class: Class 2
Regulation: 21 CFR 866.5340
Advisory panel: Immunology
Date received: 1987-09-15
Decision date: 1987-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Foster City, CA, US

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