FDA Device Intelligence
Home › GenBio › ImmunoFA Toxoplasma IgG

ImmunoFA Toxoplasma IgG

GenBio · Model 800-1200 · UDI-DI 00613745012001

GLZ
1
510(k) clearances
0
Adverse events
0
Recalls
3
Facilities

Description

The ImmunoFA Toxo IgG Test is an immunofluorescence test for the detection and titration of IgG antibodies to Toxoplasma gondii in human serum. This product is not FDA cleared (approved) for use in testing (i.e., screening) blood or plasma donors.

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.