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: QJI FDA class 2

Interoperable Automated Glycemic Controller

Clinical Chemistry

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The Interoperable Automated Glycemic Controller is a Class 2 Clinical Chemistry device that automatically calculates drug doses based on glucose and other physiological inputs and commands delivery from a connected infusion pump, 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 QJI. The device is not an implant and is not flagged as life-sustaining.

510(k) Clearances

14 matches
K Number
Device Name
Control-IQ+ technology
Control-IQ+ technology
SmartAdjust™ Technology
SmartAdjust(TM) technology
CamAPS FX
DEKA Loop
Control-IQ Technology
iLet® Dosing Decision Software
iLet® Dosing Decision Software
Tidepool Loop
SmartAdjust(TM) technology
SmartAdjust technology
Control-IQ Technology
Control-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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