FDA applicant

Medical Infusion Technologies, Inc.

Orchard Park, NY2 decisions1997–19990 recalls

FDA records 2 decisions for Medical Infusion Technologies, Inc. (Orchard Park, NY) from 1997 to 1999: 2 510(k) clearances. Most are in product codes MEB (Pump, Infusion, Elastomeric) and KNT (Tubes, Gastrointestinal (And Accessories)). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Medical Infusion Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Infusion Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Infusion Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?