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: JFL FDA class 2

Ph Rate Measurement, Carbon-Dioxide

Clinical Chemistry

View full classification →

pH Rate Measurement for Carbon Dioxide is a clinical chemistry test system that determines carbon dioxide concentration in blood or other specimens through pH-based measurement methods, supporting assessment of acid-base balance and respiratory function. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification and adherence to general and special controls. The product code is JFL, regulated under 21 CFR 862.1160, within the Clinical Chemistry medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

28 matches
K Number
Device Name
i-STAT CHEM8+ cartridge with the i-STAT 1 System
GENCHEM CO2 ACID REAGENT
MODIFICATION TO SYNCHRON LX CLINICAL CHEMISTRY SYSTEMS (LX20 AND LX20 PRO)
SIGMA DIAGNOSTICS CO2 ACID REAGENT
SIGMA DIAGNOSTICS CO2ALKALINE BUFFER
SIGMA DIAGNOSTICS ELECTROLYTE BUFFER
NOVA 16 ANALYZER (MODIFICATION POINT OF CARE USAGE)
SIGMA ELECTROLYTE REFERENCE REAGENT
SIGMA CO2 ALKALINE BUFFER REAGENT
SIGMA CO2 ACID REAGENT
SIGMA ELECTROLYTE BUFFER
HI CHEM CO2 ALKALINE BUFFER REAGENT KIT,PROD#88813
HI CHEM CO2 ACID REAGENT KIT,PRODUCT NUMBER 88812
NIIC MODEL: DX901 ASPIRATION SYSTEM
SYNCHRON EL-ISE(TM) ELECTROLYTE SYSTEMS
BICARBONATE REAGENTS PRODUCT #7713 & #7714
CARBON DIOXIDE REAGENT KIT
REPLACEMENT PARTS NOVA ELECTROLYTE ANAL
FERMCOTEST CO2 REAGNET
LIQUIZYME CO2REAGENT SET
ASTRA
BAKER DIAG. ULTRARATE CO2 REAGENT KIT
NSI CARBON DIOXIDE REAGENT KIT
CARBON DIOXIDE CUP REAGENT & REF.RGT.
NOVA 3+3 CHLORIDE/TOTAL CARBON DIOXIDE
CO2 CUP REAGENT
CO2 REFERENCE REAGENT
STAT/LYTE ANALYZER

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.

Popular Product Codes

Commonly searched