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: QJS FDA class 2

Interoperable Automated Glycemic Controller, Insulin Suspend

Clinical Chemistry

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The Interoperable Automated Glycemic Controller, Insulin Suspend is a Class 2 Clinical Chemistry device that temporarily suspends and resumes insulin infusion from a connected infusion pump based on specified glucose thresholds, designed to reliably and securely communicate with digitally connected devices to maintain glycemic control. It requires 510(k) clearance and is regulated under 21 CFR 862.1356, reviewed by the Clinical Chemistry panel. The product code is QJS. The device is not an implant and is not flagged as life-sustaining.

510(k) Clearances

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K Number
Device Name
Basal-IQ Technology

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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