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FDA 510(k)

Da Vinci Monopolar and Bipolar Adapters (378896)

K-Number: K241621 · 2024-08-02

ApplicantIntuitive Surgical
Decision Date2024-08-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Da Vinci Monopolar and Bipolar Adapters (378896) is a medical device manufactured by Intuitive Surgical. It received FDA 510(k) clearance on 2024-08-02 under approval number K241621. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Da Vinci Monopolar and Bipolar Adapters (378896)?

Da Vinci Monopolar and Bipolar Adapters (378896) is a medical device that received FDA 510(k) clearance on 2024-08-02. It is manufactured by Intuitive Surgical. The 510(k) number is K241621.

When was Da Vinci Monopolar and Bipolar Adapters (378896) approved by the FDA?

Da Vinci Monopolar and Bipolar Adapters (378896) received FDA 510(k) clearance on 2024-08-02, under approval number K241621.

What company makes Da Vinci Monopolar and Bipolar Adapters (378896)?

Da Vinci Monopolar and Bipolar Adapters (378896) is manufactured by Intuitive Surgical.

What is the FDA product code for Da Vinci Monopolar and Bipolar Adapters (378896)?

The FDA product code for Da Vinci Monopolar and Bipolar Adapters (378896) is GEI.

Related Clinical Trials

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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.

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