FDA applicant

Infusaid Corp.

Norwood, MA8 decisions1983–19910 recalls

FDA records 8 decisions for Infusaid Corp. (Norwood, MA) from 1983 to 1991: 8 510(k) clearances. Most are in product codes LJT (Port & Catheter, Implanted, Subcutaneous…) and DYB (Introducer, Catheter). 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 Infusaid Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Infusaid Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Infusaid Corp.

Which product codes does it file in?

What has FDA decided for it lately?