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: DPM FDA class 1

Columns, Liquid Chromatography

Clinical Chemistry

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Columns for Liquid Chromatography are laboratory consumables consisting of packed chromatographic columns used in liquid chromatography instruments to separate analytes in clinical chemistry testing. They are a Class 1 device subject to general controls only, with no premarket notification required. The product code is DPM, regulated under 21 CFR 862.2260, within the Clinical Chemistry specialty. No special regulatory flags apply.

510(k) Clearances

16 matches
K Number
Device Name
TOX PERFECT B TUBES AND REAGENTS
HIGH PRESSURE INERT PLASTIC COLUMNS FOR CLIN. USE
LIQUID CHROMATOGRAPHY COLUMNS
ADVANCED PURIFICATION GLASS COLUMN
LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBE
LIQUID CHROMATOGRAPHY COLUMNS HISEP COLUMN & GUARD
LIQUID CHROMATO. COLUMNS
SEP-PAK CARTRIDGES (LIQUID CHROMATOGRAPHY)
LIQUID CHROMATOGRAPHY COLUMNS
LIQUID CHROMATOGRAPHY COLUMNS
LIQUID CHROMATOGRAPHY COLUMNS;ION EXCH
PRP-1 REVERSED PHASE COLUMNS FOR HPLC
LIQUID CHROMATOGRAPHY (HPLC) COLUMNS
LIQUID CHROMATOGRAPHY COLUMNS
LIQUID CHROMATOGRAPHY COLUMNS
MAX L SYSTEM

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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