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: GGK FDA class 1

Products, Red-Cell Lysing Products

Hematology

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Red-Cell Lysing Products (product code GGK) are hematology reagents used to selectively destroy red blood cells in blood samples, facilitating the isolation and counting of white blood cells or other cellular components in automated or manual analysis. This device is classified as FDA Class 1, the lowest risk tier, subject to general controls only and not requiring premarket notification. Regulated under 21 CFR 864.8540 in the Hematology specialty (HE), this device carries no special regulatory flags.

510(k) Clearances

29 matches
K Number
Device Name
COULTER CLONE QUICK STAIN WHOLE BLOOD LYSE-II
KVM HEMOGLOBIN LYSING REAGENT
FISHER DIAGNOSTICS HEMATALL III LAS REAGENT
CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG.
PIASTRINIT
HEMOLYSE
NSI LYSING-D REAGENT -4000 ML
LASER-LYSE
ACETIC ACID 1% V/V
ACETIC ACID, 5% V/V
ACETIC ACID, 3% V/V
ACETIC ACID 2% V/V
IDL-LYSING REAGENT
LYSING & HEMOGLOBIN REAGENT
LYSE-TEC
THROMBO PLUS
LYSING & HEMOGLOBIN S-REAGENT J & S
LYSING REAGENT
LYSIS +
RED CELL LYSING REAGENT 78N 1915-1
CDL AUTO-LYSING REAGENT
CDL LYSING REAGENT
ELUAID
SERA-PAK TOTAL PROTEIN REAGENT
FLUID, RHEMOX W LYSING
REAGENT, LYSING AND HEMOGLOBIN
HEMOLYSE
CYMET-AUTOMATED
ISOTONIC DILUENT AF

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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