FDA 510(k)

LCCS VC-S RF Cannula

K-Number: K191293 · 2020-01-24

Decision Date2020-01-24

Product CodeGXI

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

LCCS VC-S RF Cannula is a medical device manufactured by Lccs Products Limited. It received FDA 510(k) clearance on 2020-01-24 under approval number K191293. 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 LCCS VC-S RF Cannula?

LCCS VC-S RF Cannula is a medical device that received FDA 510(k) clearance on 2020-01-24. It is manufactured by Lccs Products Limited. The 510(k) number is K191293.

When was LCCS VC-S RF Cannula approved by the FDA?

LCCS VC-S RF Cannula received FDA 510(k) clearance on 2020-01-24, under approval number K191293.

What company makes LCCS VC-S RF Cannula?

LCCS VC-S RF Cannula is manufactured by Lccs Products Limited.

What is the FDA product code for LCCS VC-S RF Cannula?

The FDA product code for LCCS VC-S RF Cannula is GXI.

Other Devices by Lccs Products Limited

K152642LCCS Disposable RF Electrode, LCCS Reusable RF Electrode

Related Devices (Code: GXI)

K163236COOLIEF Cooled Radiofrequency KitHalyard Health, Inc. K152642LCCS Disposable RF Electrode, LCCS Reusable RF ElectrodeLccs Products Limited K153272INTRACEPT Flexible Bi-Polar RF Probe and Easy Access Instrument SetRelievant Medsystems K170827INTRACEPT Intraosseous Nerve Ablation SystemRelievant Medsystems K170708OWL RF INSULATED CANNULAEDiros Technology, Inc. K163461Coolief* Cooled RF ProbeHalyard Health, Inc.

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.