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: LDM FDA class 1

Instrumentation, High Pressure Liquid Chromatography

Clinical Chemistry

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High pressure liquid chromatography instrumentation for clinical use is a laboratory instrument platform used in clinical chemistry to separate, identify, and quantify analytes in patient specimens with high resolution and sensitivity, supporting a wide range of diagnostic assays. It is classified as FDA Class 1, the lowest risk tier, requiring only general controls with no premarket notification needed. The product code is LDM, regulated under 21 CFR 862.2260, in the Clinical Chemistry specialty. No special risk flags apply.

510(k) Clearances

19 matches
K Number
Device Name
CDM
ALLIANCE 2690 SEPARATIONS MODULE
BIO-RAD CLINICAL DATA MANAGEMENT SYSTEM
WATERS(TM) LC MODULE I FOR CLINICAL USE
WATERS 717 AUTOSAMPLER
MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE
MODEL 250 LIQUID CHROMOTAGRAPHY PUMP
HIGH PRESSURE LIQUID CHROMATOGRAPHY SYSTEM
WATERS 650 ADVANCED PROTEIN PURIFICATION SYSTEM
ISOPURE LC SYSTEM
WATERS 740 DATA MODULE-PLOTTER INTEGRATOR
WATERS 460 LIQUID CHROMATOGRAPHY ELECTROCHEMICAL D
REPORTING INTEGRATOR 3392A
LIQUID CHROMATOGRAPH 1090 SERIES
SERIES 10 LIQUID CHROMOTOGRAPH
SERIES 4 LIQUID CHROMATOGRAPH
MODEL LC-85 UV DETECTOR
3390A REPORTING INTEGRATOR
PREP I AUTOMATED SAMPLE PROCESSOR

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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