510(k) Report

FDA applicant

Timex Medical Products Corp.

Mchenry, IL5 decisions1982–19840 recalls

FDA records 5 decisions for Timex Medical Products Corp. (Mchenry, IL) from 1982 to 1984: 5 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). 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 Timex Medical Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Timex Medical Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Timex Medical Products Corp.’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