510(k) Report

FDA applicant

Diversified Chiropractic Systems

Olathe, KS2 decisions1987–19880 recalls

FDA records 2 decisions for Diversified Chiropractic Systems (Olathe, KS) from 1987 to 1988: 2 510(k) clearances. Most are in product codes LIH (Interferential Current Therapy) and IPF (Stimulator, Muscle, Powered). 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, neurology panel, where it files most

How often FDA has decided Diversified Chiropractic Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diversified Chiropractic Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Diversified”

FDA records each applicant name separately; these may or may not be the same firm.