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IFA L. pneumophila Direct FA Test System

ZEUS SCIENTIFIC, INC. · Model FA12001 · UDI-DI 00845533001663

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

Description

The ZEUS IFA Legionella pneumophila Direct Fluorescent Antibody detection reagents are designed for the detection of Legionella (Groups 1 – 6) bacteria in various patient specimens, and are for In Vitro diagnostic use.

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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.