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: JKR FDA class 2

Radioimmunoassay, Calcitonin

Clinical Chemistry

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This device is a radioimmunoassay system used to measure calcitonin levels in patient serum, used in the diagnosis and monitoring of medullary thyroid carcinoma and other conditions affecting calcium metabolism and thyroid C-cell function. It is classified as FDA Class 2, requiring 510(k) premarket notification to demonstrate substantial equivalence, and falls within the Clinical Chemistry specialty under 21 CFR 862.1140. This device is eligible for third-party 510(k) review.

510(k) Clearances

19 matches
K Number
Device Name
ADVIA Centaur Calcitonin (CALCT) assay
ELECSYS CALCITONIN; IMMUNOASSAY, CALSET, CALCHECK 5; ELECSYS PRECICONTROL VARIA 3
CALCITONIN IMMUNORADIOMETRIC ASSAY (IRMA) (COATED TUBE VERSION)
IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL
CALCITONIN
SANGUI BIOTECH, INC. CALCITONIN ELISA KIT
NICHOLS ADVANTAGE CHEMILUMINESCENCE CALCITONIN KIT
SCANTIBODIES CALCITONIN IMMUNORADIOMETRIC ASSAY (COATED BEAD TECHNOLOGY)
CALCITONIN IMMUNOASSAY KIT
ELSA-HCT
DSL ULTRA-SENSITIVE CALCITONIN RIA (DSL 5200)
CALCITONIN KIT MITSUBISHI YUKA
MODIFIED CALCITONIN RIA KIT DSL #1200
CALCITONIN RIA KIT
DOUBLE ANTIBODY CALCITONIN RIA KIT
CALCITONIN RIA KIT
CALCITONIN RADIOIMMUNOASSAY KIT
CALCITONIN RIA TEST KIT, DLS 1200
CALCITONIN 125

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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