510(k) Report

FDA applicant

Mcpherson Enterprises, Inc.

Tampa, FL3 decisions1982–20060 recalls

FDA records 3 decisions for Mcpherson Enterprises, Inc. (Tampa, FL) from 1982 to 2006: 3 510(k) clearances. Most are in product codes DXC (Clamp, Vascular) and FOZ (Catheter, Intravascular, Therapeutic…). 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 Mcpherson Enterprises, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mcpherson Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • DXCClamp, Vascular2decisions
  • FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K062474Smithwick Carotid ShuntMcpherson Enterprises, Inc. · 20061cites it

What has FDA decided for it lately?

  • K061484Modification to: Smithwick Carotid ShuntMcpherson Enterprises, Inc. · 2006
  • K062474Smithwick Carotid ShuntMcpherson Enterprises, Inc. · 2006
  • K823565Multi-Lumen Intravenous CatheterMcpherson Enterprises, Inc. · 1982

All 3 as Mcpherson Enterprises, Inc. →