FDA applicant

Clinical Convenience Products, Inc.

Madison, WI6 decisions1979–19940 recalls

FDA records 6 decisions for Clinical Convenience Products, Inc. (Madison, WI) from 1979 to 1994: 6 510(k) clearances. Most are in product codes JXA (Kit, Screening, Urine) and JSI (Culture Media, Selective And Differential). 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, microbiology panel, where it files most

How often FDA has decided Clinical Convenience Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clinical Convenience Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Clinical Convenience Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?