FDA applicant

In Vitro Technologies, Inc.

Arlington, TX7 decisions1987–19920 recalls

FDA records 7 decisions for In Vitro Technologies, Inc. (Arlington, TX) from 1987 to 1992: 7 510(k) clearances. All are in product code DHB (System, Test, Radioallergosorbent (Rast)…). 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, immunology panel, where it files most

How often FDA has decided In Vitro Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for In Vitro Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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In Vitro Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?