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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 the device name listed in this FDA 510(k) record. The listed applicant is Lccs Products Limited. It received FDA 510(k) clearance on 2020-01-24 under 510(k) 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. The listed applicant is Lccs Products Limited. The 510(k) number is K191293.

When did LCCS VC-S RF Cannula receive FDA 510(k) clearance?

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

Who is the listed applicant for LCCS VC-S RF Cannula?

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

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 records listing Lccs Products Limited as applicant

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.

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.

Official Source

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