FDA applicant

Vascular Products, Inc.

Tarpon Springs, FL3 decisions1982–19910 recalls

FDA records 3 decisions for Vascular Products, Inc. (Tarpon Springs, FL) from 1982 to 1991: 3 510(k) clearances. Most are in product codes DWZ (Device, Biopsy, Endomyocardial) and DTB (Permanent Pacemaker Electrode). 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 Vascular Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vascular Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Vascular Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?