510(k) Report

FDA applicant

Western Medical Equipment Corp.

Lafayette, CO1 decision1987–19870 recalls

FDA records 1 decision for Western Medical Equipment Corp. (Lafayette, CO) in 1987: 1 510(k) clearance. All are in product code FLL (Continuous Measurement Thermometer). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Western Medical Equipment Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Western Medical Equipment Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Western”

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