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: FJG FDA class 2

Dialyzer, Parallel Flow

Gastroenterology, Urology

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The Parallel Flow Dialyzer is a hemodialysis device in which blood and dialysate flow in parallel channels separated by a semipermeable membrane, enabling diffusion of uremic solutes from blood into dialysate during renal replacement therapy. It is classified as FDA Class 2, requiring 510(k) premarket clearance, and is considered life-sustaining or life-supporting. The product code is FJG, regulated under 21 CFR 876.5820, within the Gastroenterology, Urology specialty.

510(k) Clearances

36 matches
K Number
Device Name
GAMBRO LUNDIA PRO 100, 500, 600 DIALYZERS
GAMBRO LUNDIA PRO 200 DIALYZER
DEXTROLYTE II PERITONEAL DIALYSIS 48-3028-9
GAMBRO LUNDIA ALPHA HEMODIALYZERS
HEMOSPAL KITS A1, A2D, AO, & A1D
TENCKHOFF PERITONEAL DIALYSIS KIT
GAMBRO LUNDIA 10-1L, 1N, 1H, 3H, 4N, 4H, 5H, 6N
GAMBRO LUNDIA PRO 3 & 5 DIALYZER
COBE PPD 1.3L, #18-520-009
COBE PPD 1.9
EXP 200 PARALLEL PLATE DIALYZER
EXP 600 PARALLEL PLATE DIALYZER
COBE PPD .8
CYBER 80 HEMODIALYZER
CYBER 120 HEMODIALYZER
NIKKISO ND-14 PARALLEL FLOW DIALYZER
EXTRACORPOREAL'S EXP 400 PARALLEL PLATE
GAMBRO LUNDIA PLATE DISP. DIALYZER
THE BRAVO NEW PARALLEL FLOW DIALYZER
ISONEPHROS-PEDIATRIC, STANDARD, OPTIMUM
CYBER 120 HEMODIALYZER
LUNDIA PLATE DISP.
GAMBRO LUNDIA PLATE DIALYZER
EXTRACORPOREAL'S MODEL EX-85 DIALYZER
HEMODIALYZERS RP-510 AND RP-514
HEMOCLEAR U-NEPHROS 1.0 DIALYZER
HD CAPILLARY FILM DIALYZER, MODEL 1001
DIALYZER, MODEL F.M.D 150
DIALYZER, MAGNIFLO 100 PARALLEL PLATE
DIALYZER, PARALLEL FLOW DISPOSABLE
LUNDIA PLATE DISPOSABLE DIALYZER
RP-510/RP-514 PARALLEL PLATE DIALYZERS
DIALYZER STANDARD, CODE 5DM1780
PARALLEL PLATE DIALYZERS
DIALYZER, ULTRADIFFUSER, DISPOSABLE
PARALLEL PLATE DIALYZER

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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