FDA applicant

Medical Testing System, Inc.

Mchenry, IL5 decisions1977–19810 recalls

FDA records 5 decisions for Medical Testing System, Inc. (Mchenry, IL) from 1977 to 1981: 5 510(k) clearances. Most are in product codes LDF (Electrode, Pacemaker, Temporary) and KNA (Instrument, Manual, Specialized…). 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, cardiovascular panel, where it files most

How often FDA has decided Medical Testing System, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Testing System, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Testing System, Inc.

Which product codes does it file in?

What has FDA decided for it lately?