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: JFP FDA class 2

Electrode, Ion Specific, Calcium

Clinical Chemistry

View full classification →

An Ion-Specific Electrode for Calcium is a clinical chemistry instrument that uses selective ion electrodes to measure ionized calcium concentration in blood or other specimens, providing data critical for diagnosing calcium metabolism disorders and guiding clinical management. It is classified as FDA Class 2 (moderate risk), subject to general and special controls, and requires 510(k) premarket notification. The product code is JFP, regulated under 21 CFR 862.1145, within the Clinical Chemistry medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

29 matches
K Number
Device Name
i-STAT CG8+ cartridge with the i-STAT 1 System
i-STAT CHEM8+ cartridge with the i-STAT 1 System
Stat Profile Prime ES Comp Plus Analyzer System
EasyLyte Na/K/Cl/Ca Analyzer
AVL OPTI CRITICAL CARE ANALYZER
AVL 9181 ELECTROLYTE ANALYZER
EASYLYTE CALCIUM/CHLORIDE ANALYZER
AVL 9180 ELECTROLYTE ANALYZER
STAT PROFILE ULTRA F,G,H,I,J, AND K ANALYZERS
EASY LYTE CALCIUM ANALYZER
AVL 988-4 ELECTROLYTE ANALYZER
I-STAT IONIZED CALCIUM TEST
ELECTRODE, ION SPECIFIC
LYTENING TM 6/R
EOS IONIZED CALCIUM TEST CARD
CALCIUM AND PH ELECTROLYTE ANALYZER
IL PHOENIX, MODEL 900, CHEMISTRY/ELECTROLYTE ANALY
LYTENING 6 SODIUM/POTASSIUM/IONIZED CALCIUM ANALYZ
MICROLYTE 7
'MICROLYTE 4/5'
IONIZED CALCIUM AND BLOOD PH TESTCARDS
CORNING CALCIUM PH ANALYZER 634
NOVA 7 TOTAL CALCIUM/IONIZED CALCIUM
NOVA 8 IONIZED CALCIUM/PH ANALYZER
SODIUM/POTASSIUM/IONIZED CALCIUM ANALYZ
MODEL AM 722
MINIATURE ION SELECTIVE ELECTRODES
ICA1 IONIZED CALCIUM ANALYZER
NOVA 2 IONIZED CALCIUM 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