FDA applicant

Viratest Intl., Inc.

San Antonio, TX3 decisions1994–19960 recalls

FDA records 3 decisions for Viratest Intl., Inc. (San Antonio, TX) from 1994 to 1996: 3 510(k) clearances. Most are in product codes KIR (Cells, Animal And Human, Cultured) and JSM (Culture Media, Non-Propagating Transport). 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, hematology panel, where it files most

How often FDA has decided Viratest Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Viratest Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Viratest Intl., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Viratest Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?