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FDA 510(k)

Vesta RF Cannula

K-Number: K190259 · 2020-02-07

ApplicantBiomerics
Decision Date2020-02-07
Product CodeGXI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Vesta RF Cannula is the device name listed in this FDA 510(k) record. The listed applicant is Biomerics. It received FDA 510(k) clearance on 2020-02-07 under 510(k) 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. The listed applicant is Biomerics. The 510(k) number is K190259.

When did Vesta RF Cannula receive FDA 510(k) clearance?

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

Who is the listed applicant for Vesta RF Cannula?

The FDA 510(k) record lists Biomerics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vesta RF Cannula?

The FDA product code for Vesta RF Cannula is GXI.

Related Devices (Code: GXI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253907Disposable Radiofrequency CannulaABBOTT MEDICALK251802STAR RF Ablation SystemMerit Medical Systems, Inc.K251243OneRF Trigeminal Nerve Radiofrequency ProbesNeuroone Medical Technologies Corp.K242841Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)ABBOTT MEDICALK250213OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Single Kit); OptaBlate BVN Intraosseous Nerve Ablation System (10mm Probe Dual Kit)Stryker InstrumentsK241367RF CannulaShanghai Samedical & Plastic Instruments Co., Ltd.

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.

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