510(k) Report

FDA applicant

Milton Roy Co. Analytical

Mchenry, IL2 decisions1977–19770 recalls

FDA records 2 decisions for Milton Roy Co. Analytical (Mchenry, IL) in 1977: 2 510(k) clearances. All are in product code FKP (System, Dialysate Delivery, Single Patient). 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 Milton Roy Co. Analytical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Milton Roy Co. Analytical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Milton”

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