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FDA 510(k)

da Vinci E-200 Electrosurgical Generator

K-Number: K231212 · 2023-06-21

ApplicantIntuitive Surgical
Decision Date2023-06-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

da Vinci E-200 Electrosurgical Generator is a medical device manufactured by Intuitive Surgical. It received FDA 510(k) clearance on 2023-06-21 under approval number K231212. 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 E-200 Electrosurgical Generator?

da Vinci E-200 Electrosurgical Generator is a medical device that received FDA 510(k) clearance on 2023-06-21. It is manufactured by Intuitive Surgical. The 510(k) number is K231212.

When was da Vinci E-200 Electrosurgical Generator approved by the FDA?

da Vinci E-200 Electrosurgical Generator received FDA 510(k) clearance on 2023-06-21, under approval number K231212.

What company makes da Vinci E-200 Electrosurgical Generator?

da Vinci E-200 Electrosurgical Generator is manufactured by Intuitive Surgical.

What is the FDA product code for da Vinci E-200 Electrosurgical Generator?

The FDA product code for da Vinci E-200 Electrosurgical Generator is GEI.

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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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