510(k) Report

FDA applicant

Cathra International, Inc.

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Cathra International, Inc. (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code LOP (Solution, Antimicrobial). 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 Cathra International, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cathra International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cathra International, 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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