FDA applicant

Ansley Medical Products, Inc.

Dallas, TX5 decisions1992–19930 recalls

FDA records 5 decisions for Ansley Medical Products, Inc. (Dallas, TX) from 1992 to 1993: 5 510(k) clearances. Most are in product codes KMK (Device, Intravascular Catheter Securement) and KKX (Drape, Surgical, Antimicrobial). 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 Ansley Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ansley Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ansley Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?