FDA applicant

Dna Medical, Inc.

Mchenry, IL5 decisions1982–19830 recalls

FDA records 5 decisions for Dna Medical, Inc. (Mchenry, IL) from 1982 to 1983: 5 510(k) clearances. Most are in product codes FPK (Tubing, Fluid Delivery) and LDR (Controller, Infusion, Intravascular, Electronic). 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 Dna Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dna Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dna Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?