FDA applicant

Dilab, Inc.

Miami, FL11 decisions1985–19870 recalls

FDA records 11 decisions for Dilab, Inc. (Miami, FL) from 1985 to 1987: 11 510(k) clearances. Most are in product codes CDW (Diacetyl-Monoxime, Urea Nitrogen) and CGO (Lieberman-Burchard/Abell-Kendall…). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

No FDA decision for Dilab, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dilab, Inc.

Which product codes does it file in?

What has FDA decided for it lately?