510(k) Report

FDA applicant

Norton Texas Medical Products

Mchenry, IL4 decisions1983–19840 recalls

FDA records 4 decisions for Norton Texas Medical Products (Mchenry, IL) from 1983 to 1984: 4 510(k) clearances. Most are in product codes JOL (Catheter And Tip, Suction) and DTR (Heat-Exchanger, Cardiopulmonary Bypass). 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, cardiovascular panel, where it files most

How often FDA has decided Norton Texas Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Norton Texas Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Norton”

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