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: FIN FDA class 2

Tank, Holding, Dialysis

Gastroenterology, Urology

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The Dialysis Holding Tank is a reservoir component of a hemodialysis system used to store dialysate solution before it is delivered to the dialyzer during treatment. It is classified as FDA Class 2, requiring 510(k) premarket notification, and is eligible for third-party 510(k) review. The product code is FIN, regulated under 21 CFR 876.5820, within the Gastroenterology, Urology specialty.

510(k) Clearances

18 matches
K Number
Device Name
TANGO3 WATER STORAGE TANK WITH OZONE DISINFECTION SYSTEM
AMERIWATER OZONE DISINFECTION SYSTEM
BICARB MIXING AND DISTRIBUTION SYSTEM
TANGO3 WATER STORAGE TANK WITH OZONE DISINFECTION SYSTEM
DIALYSIS SERVICES, INC., TYPHOON BICARB MIXING AND DISTRIBUTION SYSTEM
AMERIWATER SOLUTION MIX AND DISTRIBUTION SYSTEM FOR HEMODIALYSIS
USFILTER BICARBONATE MIXING AND DISPENSING (BICARB) SYSTEM
BIPRO MODEL SDS-CB200
BICARD MIXING SYSTEM
OSMONICS SOLUTION DELIVERY SYSTEM
MAR COR SERVICES BICARB SYSTEM
PURE WATER, INC.'S BICARB MIX, STORAGE AND DISTRIBUTION SYSTEM
PURE WATER INC'S ACIDIFIED STORAGE AND DISTRIBUTION SYSTEM WITH OPTIONAL REMOTE FILL
SODIUM BICARBONATE MIXING/DELIVERY SYSTEM, AND THE CONCENTRATE DELIVERY SYSTEM
G.E.M. WATER SYSTEMS, INTERNATIONAL
DIALYSIS MIXING & HOLDING TANK
NATURALYTE MIXER
BCM DRY PACK BICARBONATE MIXER

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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