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: NHG FDA class 2

Enzyme Immunoassay, Cortisol, Salivary

Clinical Chemistry

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The Enzyme Immunoassay, Cortisol, Salivary (product code NHG) is an in vitro diagnostic kit for the quantitative measurement of cortisol in saliva, used to assess adrenal function, stress response, and conditions such as Cushing's syndrome or adrenal insufficiency, as described in its definition. It is classified as an FDA Class 2 device within the Clinical Chemistry specialty, requiring 510(k) premarket clearance. No specific regulation number has been assigned to this product code. The device is not flagged as an implant or life-sustaining device.

510(k) Clearances

7 matches
K Number
Device Name
Cortisol Saliva Luminescence Immunoassay
PANTEX AM/PM SALIVARY CORTISOL ENZYME IMMUNOASSAY
ELECSYS CORTISOL TEST SYSTEM
ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY CORTISOL
ELECSYS CORTISOL TEST SYSTEM, ADDITION OF SALIVA SAMPLE TYPE
HIGH SENSITIVITY CORTISOL ENZYME IMMUNOASSAY
HIGH SENSITIVITY CORTISOL ENZYME IMMUNOASSAY, MODEL 1-0101/1-0102

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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