FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Control-IQ+ technology

K Number: K260429 · Decision Apr 24, 2026
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
19
Applicant Total
25
Review Days
73

Basic Information

Device Name
Control-IQ+ technology
K Number
K260429
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1356
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tandem Diabetes Care, Inc.
Date Received
February 10, 2026
Decision Date
April 24, 2026
Product Code
QJI
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QJI Interoperable Automated Glycemic Controller

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Other Clearances by Tandem Diabetes Care, Inc.

K Number Device Name
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K250798 Control-IQ+ technology
K243823 Control-IQ+ technology
K241078 Tandem Mobi Insulin Pump with interoperable technology
K240309 Tandem Mobi insulin pump with interoperable technology
K232380 t:slim X2 Insulin Pump with Interoperable Technology
K232382 Control-IQ Technology
K233044 Tandem Mobi insulin pump with interoperable technology
K223213 Tandem Mobi Insulin Pump with Interoperable Technology
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