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FDA 510(k)

Endopath Electrosurgery Probe Plus II

K-Number: K160128 · 2016-04-28

ApplicantEthicon Endo-Surgery, LLC
Decision Date2016-04-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Endopath Electrosurgery Probe Plus II is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2016-04-28 under 510(k) number K160128. 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 2016-04-28. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K160128.

When did Endopath Electrosurgery Probe Plus II receive FDA 510(k) clearance?

Endopath Electrosurgery Probe Plus II received FDA 510(k) clearance on 2016-04-28, under 510(k) number K160128.

Who is the listed applicant for Endopath Electrosurgery Probe Plus II?

The FDA 510(k) record lists Ethicon Endo-Surgery, LLC as the applicant. This does not by itself establish the device manufacturer.

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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