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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: CIB FDA class 2

Radioimmunoassay, Angiotensin I And Renin

Clinical Chemistry

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The Radioimmunoassay, Angiotensin I and Renin test system (product code CIB) is an in-vitro diagnostic device used in clinical chemistry to measure angiotensin I and plasma renin activity using a radioimmunoassay method, supporting the evaluation of the renin-angiotensin-aldosterone system and the diagnosis of hypertension and adrenal disorders. It is classified as FDA Class 2, indicating moderate risk, and requires a 510(k) premarket notification. It falls under regulation 21 CFR 862.1085 in the Clinical Chemistry medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

16 matches
K Number
Device Name
IDS ISYS DIRECT RENIN ASSAY, IDS ISYS DIRECT RENIN CONTROL SET, AND IDS ISYS DIRECT RENIN CALIBRATION VERIFIERS
LIAISON DIRECT RENIN LIAISON CONTROL DIRECT RENIN LIAISON ENDOCRINOLOGY DILUENT
CISBIO RENIN RIA TEST
ACTIVE RENIN IRMA
NICHOLS ADVANTAGE DIRECT RENIN (CALIBRATORS, CALIBRATION VERIFIERS, CONTROLS, AND SAMPLE DILUENT)
ACTIVE RENIN IRMA MODEL NUMBER DSL-25100
BUHLMANN ANGIOSTENSIN II RIA
AI-PHOTODIAGNOSTIC
ACTIVE RENIN IMMUNORADIOMETRIC ASSAY
RIANEN ANGIOTENSIN I RADIOIMMUNOASSAY KI
RENIN RADIOIMMUNOASSAY TEST KIT
ANGIOTENSIN CONVERTING ENZYME
RENAK
ANGIOTENSIS I-SQUIBB RADIOIMMUNOASSAY
RENCTK
ANGIOTENSIN I IMMUTOPE KIT

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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