510(k) Report

FDA applicant

Prevo Micro-Mat System

Highland, NY1 decision1985–19850 recalls

FDA records 1 decision for Prevo Micro-Mat System (Highland, NY) in 1985: 1 510(k) clearance. All are in product code GKJ (Spinner, Slide, Automated). 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, hematology panel, where it files most

How often FDA has decided Prevo Micro-Mat System’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Prevo Micro-Mat System since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Prevo Micro-Mat System by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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