FDA applicant

Med-West, Inc.

Salt Lake City, UT11 decisions1983–19880 recalls

FDA records 11 decisions for Med-West, Inc. (Salt Lake City, UT) from 1983 to 1988: 11 510(k) clearances. Most are in product codes FIQ (Cannula, A-V Shunt) and LFK (Catheter, Femoral). 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 Med-West, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med-West, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Med-West, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Med-West, Inc.

Which product codes does it file in?

What has FDA decided for it lately?