FDA applicant

Cgr Medical Corp.

Mchenry, IL20 decisions1978–19840 recalls

FDA records 20 decisions for Cgr Medical Corp. (Mchenry, IL) from 1978 to 1984: 20 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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, radiology panel, where it files most

How often FDA has decided Cgr Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cgr Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cgr Medical Corp.’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

Cgr Medical Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?