510(k) Report

FDA applicant

Delta Medical Industries

Mchenry, IL27 decisions1976–19840 recalls

FDA records 27 decisions for Delta Medical Industries (Mchenry, IL) from 1976 to 1984: 27 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and DTM (Filter, Blood, Cardiopulmonary Bypass…). 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, cardiovascular panel, where it files most

How often FDA has decided Delta Medical Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Delta Medical Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Delta Medical Industries’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Delta”

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