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: JHO FDA class 1

Electrophoretic Separation, Lipoproteins

Clinical Chemistry

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Electrophoretic Separation for Lipoproteins is a clinical chemistry test system that separates lipoprotein classes in serum by electrophoresis, allowing quantification of VLDL, LDL, and HDL fractions for lipid profiling and cardiovascular disease risk assessment. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is JHO, regulated under 21 CFR 862.1475, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

26 matches
K Number
Device Name
SPIFE LIPPOROTEIN-12, MODEL 3344
HYDRAGEL 7 LIPOPROTEIN(E), PN 4114 & HYDRAGEL LIPOPROTEIN(E) 15/30 PN 4134
MODIFICATION TO LIPOPRINT SYSTEM, LDL SUBFRACTIONS
MODIFIED TO LDL/HDL CHOL DIRECT KIT-P.N. 4005, 4103,4123
SPIFE 2000/3000 LIPOPROTEIN; MODEL# 3340, 3341, 3342, 3343
LIPOPRINT SYSTEM, LDL SUBFRACTIONS
SPIFE CHOLESTEROL PROFILE KIT
REP CHOLESTEROL PROFILE KIT
HYDRAGEL-MINI LIPO KIT-PN 4093, HYDRAGEL LIPO KIT-PN 4007, HYDRAGEL LIPO MAXI KIT-PN 4207
REP CHOLESTEROL PROFILE TEMPLATE-30, -16, -8; REP VIS CHOLESTEROL
MACRALP(A) ENZYME IMMUNOASSAY KIT
REP 3 QUTO-FLUR CHOLESTEROL-30
REP FLUR CHOLESTEROL-60 KIT
RAPID ELECTROPHORESIS ANALYZER
LFS LIPOGEL ASSAY KIT
REP DIRECT-SEP CHOLESTEROL-15 KIT; CHOLESTEROL-8 KIT; CHOLESTEROL-4 KIT
REP HDL/LDL-30 KIT - CAT. NO. 3220,3221,3222
REP LIPO-8 KIT, NO. 3182/REP LIPO-16 KIT, NO. 3181
REP LIPO KIT CAT. NO 3180
TITAN GEL MULTI-SLOT LIPO-17 SYSTEM
PARAGON ELECTROPHORESIS SYS LIPOPROTEIN REAGENT TE
TITAN GEL LIPOPROTEIN ELECTROPHORESIS
PARAGON LIPOPROTEIN ELECTRO. REAG. KIT
GELMAN LIPOPROTEIN FRS SET. P/N 51213
CHOLESTEROL REAGENT SUBSTRATE SET
HDL CHOLESTEROL METHOD

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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