Extended Reservoir; MiniMed Reservoir
K-Number: K241622 · 2024-07-02
ApplicantMedtronic Minimed
Decision Date2024-07-02
Product CodeLZG
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Extended Reservoir; MiniMed Reservoir is a medical device manufactured by Medtronic Minimed. It received FDA 510(k) clearance on 2024-07-02 under approval number K241622. 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 Extended Reservoir; MiniMed Reservoir?
Extended Reservoir; MiniMed Reservoir is a medical device that received FDA 510(k) clearance on 2024-07-02. It is manufactured by Medtronic Minimed. The 510(k) number is K241622.
When was Extended Reservoir; MiniMed Reservoir approved by the FDA?
Extended Reservoir; MiniMed Reservoir received FDA 510(k) clearance on 2024-07-02, under approval number K241622.
What company makes Extended Reservoir; MiniMed Reservoir?
Extended Reservoir; MiniMed Reservoir is manufactured by Medtronic Minimed.
What is the FDA product code for Extended Reservoir; MiniMed Reservoir?
The FDA product code for Extended Reservoir; MiniMed Reservoir is LZG.
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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.