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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: KHP FDA class 1

Acid, Lactic, Enzymatic Method

Clinical Chemistry

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Enzymatic Method Lactic Acid is a clinical chemistry reagent system that uses enzymatic reactions to quantify lactic acid concentration in blood or other biological specimens, supporting the assessment of tissue oxygenation, lactate metabolism, and conditions such as lactic acidosis or sepsis. It is classified as FDA Class 1, the lowest risk category, subject to general controls only, meaning it does not require premarket notification or approval. The product code is KHP, regulated under 21 CFR 862.1450, within the Clinical Chemistry medical specialty.

510(k) Clearances

27 matches
K Number
Device Name
PICCOLO LACTATE TEST SYSTEM
RAPIDPOINT 500 BLOOD GAS ANALYER
NOVA STATSTRIP LACTATE HOSPITAL METER SYSTEM
I-STAT LACTATE TEST/I-SAT CG4+CARTRIDGE
NOVA STATSTRIP LACTATE HOSPITAL METER, NOVA STATSTRIP LACTATE TEST STRIPS
EPOC BGEM, EPOC READER, EPOC HOST, EPOC CARE-FILL CAPILLARY TUBE
IRMA SL BLOOD ANALYSIS SYSTEM LACTATE CARTRIDGE
I-STAT SYSTEM
LACTATE PRO SYSTEM
I-STAT LACTATE TEST
LACTEST I
ACCUSPORT LACTATE MONITORING SYSTEM LACTATE TEST STRIPS ACCUSPORT MONITOR
STAT PROFILE PLUS 9 ANALYZER
BECKMAN SYNCHRON LACTATE REAGENT
DIMENSION(R) LACTIC ACID METHOD
KODAK EKTACHEM DT SLIDES (LAC)
URINE COLLECTION KIT/DEVICE
SYNCHRON LACTATE REAGENT
YSI MODEL 1500 SPORT L-LACTATE ANALYZER
SIGMA PROCEDURE NO. 735
KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (LAC)
EASY-TEST LACTIC ACID (LA)
TDX REA LACTIC ACID
YSI MODEL 2372 TOTAL BLOOD LACTATE KIT
LACTATE REAGENT
DUPONT ACALACTIC ACID (LA) TEST
ROCHE LACTATE ANALYZER 640

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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