FDA 510(k)

Cobbra RF Tissue Dissector

K-Number: K160041 · 2016-03-07

Decision Date2016-03-07

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Cobbra RF Tissue Dissector is a medical device manufactured by Elliquence, LLC. It received FDA 510(k) clearance on 2016-03-07 under approval number K160041. 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 Cobbra RF Tissue Dissector?

Cobbra RF Tissue Dissector is a medical device that received FDA 510(k) clearance on 2016-03-07. It is manufactured by Elliquence, LLC. The 510(k) number is K160041.

When was Cobbra RF Tissue Dissector approved by the FDA?

Cobbra RF Tissue Dissector received FDA 510(k) clearance on 2016-03-07, under approval number K160041.

What company makes Cobbra RF Tissue Dissector?

Cobbra RF Tissue Dissector is manufactured by Elliquence, LLC.

What is the FDA product code for Cobbra RF Tissue Dissector?

The FDA product code for Cobbra RF Tissue Dissector is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.