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: GHH FDA class 2

Fibrin Split Products

Hematology

View full classification →

Fibrin Split Products (product code GHH) are hematology assay reagents used to detect fibrin degradation products (FDPs) in plasma or serum, which are markers of fibrinolytic activity and are elevated in conditions such as disseminated intravascular coagulation (DIC) and thromboembolic disorders. This device is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket notification. Regulated under 21 CFR 864.7320 in the Hematology specialty (HE), it is eligible for third-party review.

510(k) Clearances

28 matches
K Number
Device Name
DIAZYME D-DIMER ASSAY KIT,CALIBRATOR SETAND CONTROL SET
PATHFAST D-DIMER
OLYMPUS D-DIMER REAGENT, MODEL OSR6X135, OLYMPUS D-DIMER CALIBRATOR, MODEL ODR3033, OLYMPUS D-DIMER CONTROL
TINA-QUANT D-DIMER TEST SYSTEM
TRIAGE D-DIMER TEST, MODEL 98100
MODIFICATION TO TINA-QUANT D-DIMER TEST SYSTEM
MDA D-DIMER
TINA-QUANT D-DIMER TEST SYSTEM
SIMPLIFY D-DIMER, MODEL DCGK1
OPUS D-DIMER
AGEN DIMERTEST GOLD EIA
FDP - SLIDEX DIRECT
MINUTEX D-DIMER LATEX TEST
BED RED D-DIMER WHOLE BLOOD AGGLUTINATION ASSAY
ABBOTT IMX(TM) D-DIMER
ABBOTT TESTPACK(TM) D-DIMER
MODIFIED D-DI-TEST KIT
FIBRINOSTICON
DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET
D-DI TEST KIT
FDP ASSAY-20 TEST KIT
ACA FIBRIN DEGRADATION PROD ANALYTICAL TEST PACK
THROMBO SCREEEN FIBRIN DEGRADATION PRODUCT KIT
DUPONT ACA FIBRIN OGEN DEGRAD-PRODUCTS CALIBRATOR
DIMERTEST LATEX
FIBROGEN(FIBRIN SPLIT PRODUCT) ANTIGEN
FIBRIN(OGEN) DEGRADATION PRODUCTS(FDP)
FIBRO-TEC TEST KIT

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.

Popular Product Codes

Commonly searched