510(k) Report

FDA applicant

Dialysis Products, Inc.

Mchenry, IL2 decisions1983–19840 recalls

FDA records 2 decisions for Dialysis Products, Inc. (Mchenry, IL) from 1983 to 1984: 2 510(k) clearances. Most are in product codes KOC (Accessories, Blood Circuit, Hemodialysis) and FKQ (System, Dialysate Delivery, Central Multiple…). 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 Dialysis Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dialysis Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Which product codes does it file in?

  • KOCAccessories, Blood Circuit, Hemodialysis1decision
  • FKQSystem, Dialysate Delivery, Central Multiple Patient1decision

What has FDA decided for it lately?

  • K842294Dialysate AdditivesDialysis Products, Inc. · 1984
  • K833653D-LYTEDialysis Products, Inc. · 1983

All 2 as Dialysis Products, Inc. →

Other applicant names beginning “Dialysis”

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

Dialysis Services, Inc. 2Dialysis Systems, Inc. 2Dialysis Solutions, Inc. 1Dialysis Medical Solutions, LLC 1Dialysis Clinic, Inc. 1