FDA applicant

Instruments For Cardiac Research

Mchenry, IL8 decisions1977–19840 recalls

FDA records 8 decisions for Instruments For Cardiac Research (Mchenry, IL) from 1977 to 1984: 8 510(k) clearances. Most are in product codes DSI (Detector And Alarm, Arrhythmia) and DSH (Recorder, Magnetic Tape, Medical). 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 Instruments For Cardiac Research’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Instruments For Cardiac Research since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Instruments For Cardiac Research by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Instruments For Cardiac Research’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Instruments For Cardiac Research

Which product codes does it file in?

What has FDA decided for it lately?