TOXOPLASMA ANTIBODY TEST SYSTEM— 510(k) K791571

Substantially Equivalent

Zeus Scientific, Inc.

FDA 510(k) clearance K791571 for TOXOPLASMA ANTIBODY TEST SYSTEM, Substantially Equivalent on 1979-09-24. Applicant: Zeus Scientific, Inc..

Clearance details

Applicant
Zeus Scientific, Inc.
Product code
Code GLZ
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

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