FDA 510(k)

Vesta RF Cannula

K-Number: K190259 · 2020-02-07

Decision Date2020-02-07

Product CodeGXI

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Vesta RF Cannula is a medical device manufactured by Biomerics. It received FDA 510(k) clearance on 2020-02-07 under approval number K190259. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vesta RF Cannula?

Vesta RF Cannula is a medical device that received FDA 510(k) clearance on 2020-02-07. It is manufactured by Biomerics. The 510(k) number is K190259.

When was Vesta RF Cannula approved by the FDA?

Vesta RF Cannula received FDA 510(k) clearance on 2020-02-07, under approval number K190259.

What company makes Vesta RF Cannula?

Vesta RF Cannula is manufactured by Biomerics.

What is the FDA product code for Vesta RF Cannula?

The FDA product code for Vesta RF Cannula is GXI.

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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.