Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: KPF FDA class 2

System, Dialysate Delivery, Semi-Automatic, Peritoneal

Gastroenterology, Urology

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This device is a semi-automatic peritoneal dialysate delivery system used to prepare and deliver dialysis fluid for patients undergoing peritoneal dialysis to manage kidney failure. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket notification. The product code is KPF, regulated under 21 CFR 876.5630 within the Gastroenterology and Urology specialty. This device is designated as life-sustaining or life-supporting, reflecting its critical role in renal replacement therapy.

510(k) Clearances

13 matches
K Number
Device Name
RENALSOFT
RENAL LINK
CYBERREN
PACKPD PERITONEAL DIALYSIS UREA KINETIC MODELING SOFTWARE PROGRAM
TOTAL CONTAINMENT DEVICE
AMICON EQUALINE FLUID BALANCE SYSTEM
ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE
C.A.P.D. AUTOMATIC HEATER #PDC 2000 HCP
GAMBRO PERITONEAL DIALYSIS MONITOR
CYCLER W/5 OR 10 HR. FILL/DWELL TIMER
PERITONEAL DIALYSIS CYCLER MODEL PDC1000
CYLER/HEATER FOR PERITONEAL DIALYSIS
AMP AUTOMATIC CYCLER STAND

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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