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.

Product Code: FKP FDA class 2

System, Dialysate Delivery, Single Patient

Gastroenterology, Urology

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The Single-Patient Dialysate Delivery System is a machine or system that prepares and delivers dialysate solution to an individual patient's hemodialysis circuit during treatment. It is classified as FDA Class 2 (moderate risk) and requires 510(k) premarket notification. The product code is FKP, regulated under 21 CFR 876.5820 in the Gastroenterology and Urology specialty. This device is designated as life sustaining or life supporting.

510(k) Clearances

50+ matches
K Number
Device Name
NxStage Connected Health System
NXSTAGE CONNECTED HEALTH SYSTEM
NXSTAGE DOSING CALCULATOR
ONEVIEW INTERFACE
FRESENIUS ICARE MONITORING SYSTEM
STERICHEK SENSITIVE-FEED WATER AND RINSE WATER REAGENT STRIPS
CKHEMO, MODEL CKHEMO VERSION 1.0
HIGH RANGE PEROXIDE TEST STRIP
PACK H HEMODIALYSIS UREA KINETIC MODELING SOFTWARE PROGRAM
WATERCHECK REAGENT STRIP FOR CHLORINE & PEROXIDE
BIOPURE DIALYSATE CONCENTRATE MIX SYST/CONCENTRATE
SPS 1550 SINGLE NEEDLE PATIENT SYSTEM
FRESENIUS 3008/FDS-08 DIALYSATE DELIVERY SYSTEM
DRAKE WILLOCK SYSTEM 1000 DIALYSATE DELIVERY SYST
COBE CENTRY 2 BICART OPTION KIT
COBE CENTRYSYSTEM 3 BICART OPTION KIT
HOSPAL BICART RETROFIT KIT NA/MONIT S GS HEMODIAL
GAMBRO BICARBONATE MONITOR BCM 10-3
GAMBRO AK-10 DIALYSIS SYSTEM FOR HIGH FLOWS
HEMODIALYSIS SINGLE PATIENT SYSTEM (SPS) 550 VSB
FRESENIUS 2008 TOUCH PANEL CONTROL DIALYSIS SYSTEM
HEOMDIALYSIS SINGLE PATIENT SYSTEM (SPS) MODEL 650
480 HIGH-FLOW ULTRAFILTRATION CONTROL DIALYSATE
GAMBRO BICART SYSTEM
MONITRAL S GS HEMODIALYSIS SINGLE PATIENT UNIT
SINGLE-PATIENT AUTOMATIC DIALYSIS UNIT MOD. DBB-22
GAMBRO FLUID CONTROL MONITOR FCM 10-1
GAMBRO BICARBONATE MONITOR BCM 10-2
MONITRAL S
HD-SECURA HEMADIALYSIS MACHINE
BEDSIDE CONSOLE HA-57P/BLOOD & HEPARIN PUMP BIP-BH
DRAKE WILLOCK 480 UF CONTROL IDALYSATE DELIVERY SY
COBE SYSTEM 3
BSM 2000 DIALYSIS MACHINE - MODIFIED
MBM(TM) MONITRAL (R) BICARBONATE MODULE
HEMODIALYSIS SYSTEM
EXTRASENSR ULTRAFILTRATION MONITOR
B-D DRAKE WILLOCK #7000 SERIES ULTRAF
EXTRACORPOREAL'S #DM-952 DIALYSATE BYPAS
DIALYSIS CONTROL UNIT-CENTRY 2000
MODEL 7200 HEMODIALYSIS DELIVERY SYSTEM
GAMBRO AK-10-UDM-10-A ULTRADIFFUSION
MODELS DM-360 & DM-350-L SINGLE PATIENT
DIALYSATE DELIVERY SYSTEM
SUITCASE KIDNEY HEMODIALYSIS SYSTEM
SINGLE PATIENT SYSTEMS
EMODIALYSIS DEL. SYS. MODEL 7110
DYLADE, MODEL DS
DIALYSIS DELIVERY SYS., ULTIM. MODEL II
5M1352 PROPORT. DIALYSIS FLUID DELIV.ERY

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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