FDA applicant

Professional Dialysis Products

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Professional Dialysis Products (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code FKG (Tray, Start/Stop (Including Contents), Dialysis). 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 Professional Dialysis Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Professional Dialysis Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Professional Dialysis Products’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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Other applicant names beginning “Professional”

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

Professional Medical Services 19 Professional Medical Products, Inc. 9 Professional Latex Sdn Bhd 3 Professional Instruments Co. 3 Professional Positioners, Inc. 3 Professional Tape Co., Inc. 2 Professional Services For Surgeons, Ltd. 2 Professional Dental Mfg., Inc. 2 Professional Technologies Corp. 2 Professional Supplies, Inc. 2 Professional Disposables International, Inc. 1 Professional Medical Systems 1

Professional Dialysis Products

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Professional”