FDA applicant

Preco, Inc.

Oakland, NJ4 decisions1985–19850 recalls

FDA records 4 decisions for Preco, Inc. (Oakland, NJ) in 1985: 4 510(k) clearances. Most are in product codes JHJ (Agglutination Method, Human Chorionic…) and DHR (System, Test, Rheumatoid Factor). 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 Preco, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Preco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Preco, Inc.

Which product codes does it file in?

What has FDA decided for it lately?