FDA applicant
Timex Medical Products Corp.
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
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.
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