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: JIR FDA class 1

Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)

Clinical Chemistry

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This device is a clinical chemistry reagent that uses an indicator (colorimetric dye) method to detect protein or albumin in urine on a qualitative, non-quantitative basis, supporting urinalysis screening in clinical laboratories. It is classified as FDA Class 1, the lowest risk tier, subject to general controls only and exempt from premarket notification requirements. The product code is JIR, regulated under 21 CFR 862.1645, and assigned to the Clinical Chemistry medical specialty.

510(k) Clearances

38 matches
K Number
Device Name
Minuteful-kidney test
Minuteful - kidney test
Mission Urinalysis Reagent Strips (Microalbumin/Creatinine)
TECO MICROALBUMIN 2-1 COMBO STRIPS
IMMUNODIP URINARY ALBUMIN SCREEN ASSAY, CATALOGUE NUMBER 790-25
URISITE URINE COLLECTION KIT FOR MICROALBUMIN/CREATININE TESTING
IMMUNODIP URINARY ALBUMIN SCREEN, MODEL 790-01, 790-15
NEW MULTIPLES REAGENT STRIPS
MICROALBUSTIX REAGENT STRIPS (OTC)
UALB
HEALTH CHECK URI-TEST PROTEIN IN URINE
MICROALBUSTIX REAGENT STRIPS
DCLARE IMMUNODIP STICKFOR MICROALBUMINURIA
ORGENTEC MICRO-ALBUMIN EIA ASSAY
DCA 2000 + MICROALBUMIN/CREATININE ASSAY
TOTAL PROTEIN (URINE)
ORGENTEC MICRO-ALBUMIN PIN EIA ASSAY
URINE REAGENT STRIPS-3 PARAMETERS (MODIFICATION)
CHEMSTRIP MICRAL URINE TEST STRIPS
TINA-QUANT MICROALBUMIN
N-ASSAY TIA MICROALBUMIN
ENZIP URINARY MICROALBUMIN TEST
SYN ELISA MICRO ALBUMIN
TARGET MICROALBUMINURIA TEST
MICRO ALBUMIN EIA TEST KIT
CHEMSTRIP(R) MICRAL(TM) URINE TEST STRIPS
STANBIO CSF/URINE TOTAL PROTEIN TEST SET
KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT
BIOTEL MICROALBUMINURIA (TM)
DIALBUMIN
BIOTROL URINE PROTEINS REAGENT
PROGENE MICROALBUMINURIA SCREEN
BIOTROL URINE PROTEINS REAGENT
ALBUWELL
MICRO-BUMINTEST REAGENT TABLETS
DOUBLE ANTIBODY ALBUMIN FOR DETECT MICROALBUMINURI
HELENA BIOSTRIP P
KOVA STRIP 6

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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