FDA applicant

Chicago Assoc. For Retarded Citizens

Chicago, IL1 decision1990–19900 recalls

FDA records 1 decision for Chicago Assoc. For Retarded Citizens (Chicago, IL) in 1990: 1 510(k) clearance. All are in product code FXY (Hood, Surgical). 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, general and plastic surgery panel, where it files most

How often FDA has decided Chicago Assoc. For Retarded Citizens’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chicago Assoc. For Retarded Citizens since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Chicago Assoc. For Retarded Citizens by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Chicago”

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

Chicago X-Ray Systems, Inc. 4

Chicago Assoc. For Retarded Citizens

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Chicago”