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: JIL FDA class 2

Method, Enzymatic, Glucose (Urinary, Non-Quantitative)

Clinical Chemistry

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Enzymatic Method for Glucose (Urinary, Non-Quantitative) is a clinical chemistry test system using enzymatic reactions to detect the presence of glucose in urine on a non-quantitative basis, used for screening of diabetes mellitus and renal glycosuria. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification and compliance with general and special controls. The product code is JIL, regulated under 21 CFR 862.1340, within the Clinical Chemistry medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
AUTION MAX AX-4060 Urinalysis System
cobas u 601 urinalysis test system
DIP/U.S. Urine Analysis Test System
inui In-Home Urine Analysis Test System
DUS 2GP Reagent Strips, DUS 5 Reagent Strips, DUS 10 Reagent Strips
DUS R-50S (Urine Chemistry system)
iChemVELOCITY Automated Urine Chemistry System
AUTION ELEVEN Semi-Automated Urinalysis System
URITEK TC-201 URINE CHEMISTRY TEST SYSTEM
TC-THUNDERBOLT AUTOMATED URINE ANALYZER SYSTEM AND TC-THUNDERBOLT URS-10 STRIPS
URS-2GP (GLUCOSE PROTEIN) URINE STRIPS
FORESIGHT U120 URINE ANALYZER
URITEK TC-101 URINE ANALYZER, URINE REAGENT STRIPS 10, MODELS TC-101, URS-10
CLINITEK STATUS+ANALYZER AND CLINITEK STATUS CONNECT SYSTEM, MODELS 1780, 1797
COMBI SCAN 500 URINE TEST STRIP ANALYZER, MODEL A93005
COMBI SCAN100
URINE CHEMISTRY ANALYZER UR-50
CLINITEK ADVANTUS, MODEL 1420
URYXXON RELAX URINE ANALYZER
ICHEM 100 URINE CHEMISTRY ANALYZER
CYBOW 11 SERIES REAGENT STRIPS FOR URINALYSIS
URYXXON 200 URINE ANALYZER
URISCAN OPTIMA II URINE ANALYZER
CHEMVIEW-10
DIASCREEN REAGENT STRIPS FOR URINALYSIS, MODELS D122OO (2GK), D12100 (1K), D11100 (1G)
COMBI-SCREEN, MODELS 10SL AND 11SL
CHEMSTRIP 5 OB, CHEMSTRIP 7 AND CHEMSTRIP 10 MD TEST STRIPS
POCKETCHEM UA AUTION STICKS 10TA
URS-IG (GLUCOSE TEST)
URISYS 2400 URINE TEST STRIP
DIASCREEN 50 URINE CHEMISTRY ANALYZER, MODEL # 1242-00; DIASCREEN REAGENT STRIP FOR URINALYSIS, CAT. # D11000
MEDI-TEST COMBI 11
DBEST REAGENT STRIP FOR URINALYSIS
CLINISTRIP
HEALTH CHECK URI-TEST GLUCOSE IN URINE TEST
DIA SCREEN 10 WAY REAGENT STRIPS
FIRST CHOICE GLUCOSE URINE TEST STRIPS
BIOSCAN
DIA SCREEN REAGENT STRIPS
IN VITRO DIAGNOSTIC URINE REAGENT STRIPS SET
URISTRIP REAGENT STRIPS TEST FOR PROTEIN, GLUCOSE, PH AND BLOOD
URINE REAGENT STRIP-3 PARAMETERS
BIOSCAN REAGENT STRIPS
UROPAPER EIKEN 6B
UROPAPER EIKEN HAG
UROPAPER EIKEN AG
UROPAPER EIKEN GP
UROPAPER
UROPAPER EIKEN 7
UROPAPER EIKEN 8

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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