FDA applicant

Infusion Technology Intl.

Danvers, MA3 decisions1994–19950 recalls

FDA records 3 decisions for Infusion Technology Intl. (Danvers, MA) from 1994 to 1995: 3 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FIH (Pump, Infusion Or Syringe, Extra-Luminal). 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 Infusion Technology Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Infusion Technology Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Infusion”

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

Infusion Dynamics, Inc. 3 Infusion Systems Corp. 2 Infusion Devices, Inc. 1 Infusion Safety Products, Inc. 1

Infusion Technology Intl.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Infusion”