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: JIN FDA class 1

Nitroprusside, Ketones (Urinary, Non-Quant.)

Clinical Chemistry

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Nitroprusside for Ketones (Urinary, Non-Quantitative) is a clinical chemistry test system that uses the sodium nitroprusside reaction to detect the presence of ketone bodies in urine on a non-quantitative basis, used for screening in diabetic ketoacidosis and other ketotic states. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is JIN, regulated under 21 CFR 862.1435, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

24 matches
K Number
Device Name
KetoSens BT Blood B-Ketone Monitoring System
VivaChek Blood Glucose and B-Ketone Monitoring System
KET-1 Blood Ketone Monitoring System
TD-4140 Smart Dongle Blood Glucose plus B-ketone Monitoring System
KetoSens Blood B-Ketone Monitoring System, KetoSens Multi Blood B-Ketone Monitoring System
On Call Ketone Reagent Strips for Urinalysis, Healthy Me Ketone Reagent Strips for Urinalysis
PRECISION XTRA BLOOD B KETONE TEST STRIPS, OPTIUM BLOOD B KETONE TEST STRIPS
KETOCHECKS
URS-1K (KETONE TESST)
FIRST CHOICE KETONES URINE TEST STRIPS
FIRST CHOICE GLUCOSE & KETONES URINE TEST STRIPS
KETO-340 II
KETOSITE(TM)/STAT-SITE(TM)/KETOSITE(TM) LOW-HI CON
GDS ENZYMATIC B-HYDROXYBUTYRATE REAGENT MODIFIED
KETOREX SANWA STANDARDS
KETONE TEST A SANWA STANDARD
KETONE TEST B SANWA STANDARD
ABBOTT BREATH ACETONE ANALYZER
SIGMS B-HYDROXYBUTARATE PROCEDURE NO. 310-UV
KYOTEST UK URINE TEST REAGENT STRIP
GLUCOSE 3, INLAB REAGENT STRIPS-URINALY
PLAN A LIFE
HELENA BIOSTRIP K
TEST FOR KETONE IN URINE(ACETOACETIC AC

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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