FDA applicant

Catheter Corp. of America

Walker, MI1 decision1983–19830 recalls

FDA records 1 decision for Catheter Corp. of America (Walker, MI) in 1983: 1 510(k) clearance. All are in product code DYG (Catheter, Flow Directed). 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 Catheter Corp. of America’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Catheter Corp. of America since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Catheter”

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

Catheter Technology Corp. 13 Catheter Innovations, Inc. 8 Catheter Research, Inc. 8 Catheter Research C/O Burditt, Bowles & Radzius 8 Catheter Connections, Inc. 7 Catheter Robotics, Inc. 3 Catheter Precision, Inc. 2 Catheter Sciences Co. 2 The Catheter Exchange, Inc. 1 Catheter, LLC 1

Catheter Corp. of America

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Catheter”