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: FKQ FDA class 2

System, Dialysate Delivery, Central Multiple Patient

Gastroenterology, Urology

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The Central Multiple-Patient Dialysate Delivery System is a centralized system that prepares and distributes dialysate solution to multiple hemodialysis stations simultaneously within a dialysis facility. It is classified as FDA Class 2 (moderate risk) and requires 510(k) premarket notification. The product code is FKQ, 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
DIACAP ULTRA DIALYSIS FLUID FILTER
TWO TANK DISSOLUTION MODULE
MULTIPLE ARTIFICIAL KIDNEY SYSTEMS (MAKS) #IDM
KAWASUMI A.V. FISTULA SET
ACID FUCHSIN SOLUTIONS
ACTRIL FOR KIDNEY MACHINE DISINFECTANT
FOUR TANK DISSOLUTION MODULE
DRAKE WILLOCK CENTRAL DIALYSATE DELIVERY SYSTEM
MAKS CENTRAL DELIVERY SYSTEMS MODELS 11-425/11-445
AMUCHINA/DIALYZER DISINFECTANT
HEMODIALYSIS CONCENTRATE FORMULATIONS/ADDITIVES
HEMODIALYSIS CONCENTRATE FORMULATIONS/ADDITIVES
HEMODIALYSIS CONCENTRATES AND RELATED PRODUCTS
HEMODIALYSIS CONCENTRATE
RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANT
NATURALYTE BICARBONATE CONCENTRATE-DRY PACK
ALCIDE REN NEW-D
MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT
FRESENIUS A2008 HEMODIALYSIS MACHINE EXPANSION MOD
FRESENIUS HAEMODIALYSIS ;MACHINE A1008
NEPHROSS ALLEGRO H.F.
ST FAMILY OF HOLLOW FIBER DIALYZERS
DIALYSATE CONCENTRATE FOR HEMODIALYSIS-LIQUID/POWD
UNILYTE A
HEMODIAL CONCENTRATE MIXING APPARATUS
FORMACLEAR- & MULTIPLE
MONOXYCHLOROSENE WAREXIN
PACKETS FOR THE PREP OF DIALYSATES &
HEMODIALYSIS BATH CONCENTRATE SOLUTION
DIALYSATE ADDITIVES
CONCENTRATE CONDUCTIVITY METER
RENAPAK CONCENTRATE MIXING SYS.
CHEMLYTE
HEMODIAL CONCENTRATE
BIOSPAL 3000S
BIOSPAL 2400S
BIOSPAL 1200S
HOSPAL MODEL H1210
GAMMA STERIL. CAPILLARY FLOW DIALY-G15
GAMMA STERILIZED CAPILLARY FLOW DIALYZ
BICARBONATE/VARIABLE SODIUM KIT-DM-367
HEMAFLO BLOOD TUBING SETS
DISSCAP 080
CIDEX*DIALYZER DISINFECTING SOLUTION
HPF 100,200,300 CAPILLARY FLOW DIALYZ
MODEL 100 BICARBONATE CONDUCTIVITY
DISSCAP 140
DISSCAP 110
GAMBRO LUNDIA 10 3N PARALLEL FLOW DIAL
DIALYSATE CONCENTRATE

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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