510(k) Report

FDA applicant

Laboratory Products, Inc.

Mchenry, IL8 decisions1979–19830 recalls

FDA records 8 decisions for Laboratory Products, Inc. (Mchenry, IL) from 1979 to 1983: 8 510(k) clearances. Most are in product codes JIX (Calibrator, Multi-Analyte Mixture) and IFI (Sprays, Synthetic, Smear). 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 Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Laboratory Products, 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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