FDA applicant

Chesire Laboratories

Mchenry, IL4 decisions1977–19930 recalls

FDA records 4 decisions for Chesire Laboratories (Mchenry, IL) from 1977 to 1993: 4 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and JOL (Catheter And Tip, Suction). 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 hospital panel, where it files most

How often FDA has decided Chesire Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chesire Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Chesire Laboratories’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

Chesire Laboratories

Which product codes does it file in?

What has FDA decided for it lately?