FDA applicant

Pan Probe Biotech, Inc.

San Diego, CA10 decisions2001–20020 recalls

FDA records 10 decisions for Pan Probe Biotech, Inc. (San Diego, CA) from 2001 to 2002: 10 510(k) clearances. Most are in product codes DKZ (Enzyme Immunoassay, Amphetamine) and DOE (Radioimmunoassay, Morphine (125-I), Goat…). 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 toxicology panel, where it files most

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

FDA decisions per year

No FDA decision for Pan Probe Biotech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Pan Probe Biotech, Inc.

Which product codes does it file in?

What has FDA decided for it lately?