510(k) Report

FDA applicant

Laboratory Technologies, Inc.

Schaumburg, IL4 decisions1985–19930 recalls

FDA records 4 decisions for Laboratory Technologies, Inc. (Schaumburg, IL) from 1985 to 1993: 4 510(k) clearances. Most are in product codes JJJ (Counter (Beta, Gamma) For Clinical Use) and JJE (Analyzer, Chemistry (Photometric, Discrete)…). 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 Laboratory Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laboratory Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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