Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater

K-Number: K160482 · 2016-07-13

Decision Date2016-07-13
Product CodeLZG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater is a medical device manufactured by Tandem Diabetes Care, Inc.. It received FDA 510(k) clearance on 2016-07-13 under approval number K160482. The device is classified under product code LZG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater?

t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater is a medical device that received FDA 510(k) clearance on 2016-07-13. It is manufactured by Tandem Diabetes Care, Inc.. The 510(k) number is K160482.

When was t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater approved by the FDA?

t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater received FDA 510(k) clearance on 2016-07-13, under approval number K160482.

What company makes t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater?

t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater is manufactured by Tandem Diabetes Care, Inc..

What is the FDA product code for t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater?

The FDA product code for t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater is LZG.

Related Clinical Trials

Related PubMed Literature

Other Devices by Tandem Diabetes Care, Inc.

View all 22 devices →

Related Devices (Code: LZG)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.