FDA applicant
Eldeco
FDA records 5 decisions for Eldeco (Mchenry, IL) in 1976: 5 510(k) clearances. Most are in product codes DRT (Monitor, Cardiac (Incl. Cardiotachometer &…) and DXH (Transmitters And Receivers…). 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 Eldeco’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Eldeco since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Eldeco’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