K232382 is an FDA 510(k) clearance for the Control-IQ Technology. Classified as Interoperable Automated Glycemic Controller (product code QJI), Class II - Special Controls.
Submitted by Tandem Diabetes Care, Inc. (San Diego, US). The FDA issued a Cleared decision on November 3, 2023 after a review of 87 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1356 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.
Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.
View all Tandem Diabetes Care, Inc. devices
NCT04796779
Completed
Interventional
The Pediatric Artificial Pancreas (PEDAP) Trial of Control-IQ Technology in Young Children in Type 1 Diabetes
The Pediatric Artificial Pancreas (PEDAP) Trial: A Randomized Controlled Comparison of the Control-IQ Technology Versus Standard of Care in Young Children in Type 1 Diabetes
| Condition studied |
Type 1 Diabetes |
| Study design |
Parallel |
| Eligibility |
All sexes
· 24 Months+
|
| Principal investigator |
John Lum, MS |
| Sponsor |
Marc Breton
|
Started 2021-04-21
→
Primary completion 2022-04-12
→
Completed 2022-07-31
Primary outcome
Time in Range
Secondary outcome
CGM-measured Percent Above 250 mg/dL
View full study on ClinicalTrials.gov