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FDA 510(k)

Tandem Mobi Insulin Pump with interoperable technology

K-Number: K241078 · 2024-07-26

Decision Date2024-07-26
Product CodeQFG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Tandem Mobi Insulin Pump with interoperable technology is a medical device manufactured by Tandem Diabetes Care, Inc.. It received FDA 510(k) clearance on 2024-07-26 under approval number K241078. The device is classified under product code QFG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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