510(k) Report

FDA applicant

Cirs, Inc.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Cirs, Inc. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code IXG (Phantom, Anthropomorphic, Radiographic). 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 Cirs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cirs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cirs, 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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