FDA applicant

Cardio Med Supplies, Inc.

Gormley, Ontario, CA5 decisions1980–20080 recalls

FDA records 5 decisions for Cardio Med Supplies, Inc. (Gormley, Ontario, CA) from 1980 to 2008: 5 510(k) clearances. Most are in product codes LHI (Set, I.V. Fluid Transfer) and MSD (Catheter, Hemodialysis, Implanted). 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 Cardio Med Supplies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Cardio Med Supplies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?