meddevicedb.com FDA Device Reference

Control-IQ Technology

DEN190034 Class II Direct
Decision Date
2019-12-13
Sponsor / Applicant
Tandem Diabetes Care, Inc.

Technical Specification

510(k) Submission ID DEN190034
Product Code QJI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1356
Decision Date 2019-12-13
Clearance Pathway Direct

Official Documentation

No FDA summary/statement PDF is linked for this clearance in the current dataset. Consult the product code and regulation citation above to locate predicate documentation.

Clearance Summary

Control-IQ Technology received FDA 510(k) clearance under submission number DEN190034, sponsored by Tandem Diabetes Care, Inc.. The device was reviewed via the Direct premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2019-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code QJI and 21 CFR 862.1356, within the Clinical Chemistry review panel as a Class II device.