FDA applicant
Delta Medical Industries
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
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.
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) ReportOther applicant names beginning “Delta”
FDA records each applicant name separately; these may or may not be the same firm.