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FDA 510(k)

Endopath Electrosurgery Probe Plus II

K-Number: K180031 · 2018-05-07

ApplicantEthicon Endo-Surgery, LLC
Decision Date2018-05-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Endopath Electrosurgery Probe Plus II is a medical device manufactured by Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2018-05-07 under approval number K180031. 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 Endopath Electrosurgery Probe Plus II?

Endopath Electrosurgery Probe Plus II is a medical device that received FDA 510(k) clearance on 2018-05-07. It is manufactured by Ethicon Endo-Surgery, LLC. The 510(k) number is K180031.

When was Endopath Electrosurgery Probe Plus II approved by the FDA?

Endopath Electrosurgery Probe Plus II received FDA 510(k) clearance on 2018-05-07, under approval number K180031.

What company makes Endopath Electrosurgery Probe Plus II?

Endopath Electrosurgery Probe Plus II is manufactured by Ethicon Endo-Surgery, LLC.

What is the FDA product code for Endopath Electrosurgery Probe Plus II?

The FDA product code for Endopath Electrosurgery Probe Plus II 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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