510(k) Report

FDA applicant

Cyberex Corp.

Mchenry, IL4 decisions1979–19810 recalls

FDA records 4 decisions for Cyberex Corp. (Mchenry, IL) from 1979 to 1981: 4 510(k) clearances. Most are in product codes FJG (Dialyzer, Parallel Flow) and FIL (System, Dialysate Delivery, Single Pass). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Cyberex Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cyberex Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cyberex Corp.’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