Tandem Mobi Insulin Pump with interoperable technology
K-Number: K241078 · 2024-07-26
Device Summary
Frequently Asked Questions
What is the Tandem Mobi Insulin Pump with interoperable technology?
Tandem Mobi Insulin Pump with interoperable technology is a medical device that received FDA 510(k) clearance on 2024-07-26. It is manufactured by Tandem Diabetes Care, Inc.. The 510(k) number is K241078.
When was Tandem Mobi Insulin Pump with interoperable technology approved by the FDA?
Tandem Mobi Insulin Pump with interoperable technology received FDA 510(k) clearance on 2024-07-26, under approval number K241078.
What company makes Tandem Mobi Insulin Pump with interoperable technology?
Tandem Mobi Insulin Pump with interoperable technology is manufactured by Tandem Diabetes Care, Inc..
What is the FDA product code for Tandem Mobi Insulin Pump with interoperable technology?
The FDA product code for Tandem Mobi Insulin Pump with interoperable technology is QFG.
Related Clinical Trials
Related PubMed Literature
Other Devices by Tandem Diabetes Care, Inc.
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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.