510(k) Report

FDA applicant

Merchant House Scientific

Irvine, CA3 decisions1993–19940 recalls

FDA records 3 decisions for Merchant House Scientific (Irvine, CA) from 1993 to 1994: 3 510(k) clearances. All are in product code LBR (Ldl & Vldl Precipitation, Hdl). 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 Merchant House Scientific’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Merchant House Scientific since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Merchant House Scientific’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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