FDA applicant

Histo-Med, Inc.

Orange City, FL1 decision1993–19930 recalls

FDA records 1 decision for Histo-Med, Inc. (Orange City, FL) in 1993: 1 510(k) clearance. All are in product code JBB (Solubility, Hemoglobin, Abnormal). 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 Histo-Med, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Histo-Med, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Histo-Med, Inc.

Which product codes does it file in?

What has FDA decided for it lately?