MODIFIED FERRITIN ENZYME IMUNOASSAY TEST KIT— 510(k) K920046

Substantially Equivalent

Medix Biotech, Inc.

FDA 510(k) clearance K920046 for MODIFIED FERRITIN ENZYME IMUNOASSAY TEST KIT, Substantially Equivalent on 1992-01-28. Applicant: Medix Biotech, Inc..

Clearance details

Applicant: Medix Biotech, Inc.
Product code: Code DBF
Advisory panel: Immunology
Date received: 1992-01-06
Decision date: 1992-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Foster City, CA, US

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