FDA 510(k)

SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE

K-Number: K034012 · 2004-03-16

Decision Date2004-03-16

Product CodeGXI

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2004-03-16 under 510(k) number K034012. 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 SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE?

SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE is a medical device that received FDA 510(k) clearance on 2004-03-16. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K034012.

When did SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE receive FDA 510(k) clearance?

SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE received FDA 510(k) clearance on 2004-03-16, under 510(k) number K034012.

Who is the listed applicant for SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE?

The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE?

The FDA product code for SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE 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.