FDA applicant

Virus Reference Laboratory, Inc.

San Antonio, TX1 decision1992–19920 recalls

FDA records 1 decision for Virus Reference Laboratory, Inc. (San Antonio, TX) in 1992: 1 510(k) clearance. All are in product code LJB (Enzyme Linked Immunoabsorbent Assay, Rubeola Igg). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, microbiology panel, where it files most

How often FDA has decided Virus Reference Laboratory, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Virus Reference Laboratory, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Virus Reference Laboratory, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Virus Reference Laboratory, Inc.

Which product codes does it file in?

What has FDA decided for it lately?