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Toxoplasma gondii IgG

ZEUS SCIENTIFIC, INC. · Model FA8001G · UDI-DI 00845533002103

Prescription
0
510(k) clearances
0
Adverse events
0
Recalls
0
Facilities

Description

The Toxoplasma gondii IgG is designed to detect the presence of circulating T. gondii antibodies in human sera and is for In Vitro diagnostic use. This product is not FDA cleared (approved) for use in testing (i.e., screening) blood or plasma donors.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.