510(k) Report

FDA applicant

Central Solutions, Inc.

Kansas City, KS7 decisions1995–19980 recalls

FDA records 7 decisions for Central Solutions, Inc. (Kansas City, KS) from 1995 to 1998: 7 510(k) clearances. All are in product code LRJ (Disinfectant, Medical Devices). 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, general hospital panel, where it files most

How often FDA has decided Central Solutions, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Central Solutions, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Central Solutions, 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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