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: JCF FDA class 1

Lymphocyte Separation Medium

Hematology

View full classification →

A lymphocyte separation medium is a density gradient reagent used in hematology and immunology laboratories to isolate mononuclear cells, particularly lymphocytes and monocytes, from whole blood through centrifugation, enabling downstream cellular analysis and testing. It is classified as FDA Class 1, the lowest risk category, subject only to general controls without requiring premarket notification. The product code is JCF, regulated under 21 CFR 864.8500, within the Hematology medical specialty. No special flags apply to this device.

510(k) Clearances

12 matches
K Number
Device Name
LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITR
LYMPHO SEP(TM)
LEUCOPREP CELL SEPARATION TUBE
L-PHENYLALANINE METHYL ESTER HYDROCHLORIDE PME REA
DYNABEADS HLA CELL PREP II ISOLATION PRODUCT
LEUCOPREP BRAND TUBE
SEPRACELL LYMPHOCYTE SEPARATION MEDIUM
LEUCO PREP
CST
HISTOPAQUE-1077
MONO-POLY RESOLVING MEDIUM
IMMUNO-CELL IMMUNO-SEP 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.

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