FDA applicant

Steridoc Corp.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Steridoc Corp. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code KQQ (Tubing, Dialysate (And Connector)). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Steridoc Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Steridoc Corp.

Which product codes does it file in?

What has FDA decided for it lately?