FDA 510(k)

VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2

K-Number: K040638 · 2004-06-07

ApplicantVnus Medical Technologies, Inc.

Decision Date2004-06-07

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 is the device name listed in this FDA 510(k) record. The listed applicant is Vnus Medical Technologies, Inc.. It received FDA 510(k) clearance on 2004-06-07 under 510(k) number K040638. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2?

VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 is a medical device that received FDA 510(k) clearance on 2004-06-07. The listed applicant is Vnus Medical Technologies, Inc.. The 510(k) number is K040638.

When did VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 receive FDA 510(k) clearance?

VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 received FDA 510(k) clearance on 2004-06-07, under 510(k) number K040638.

Who is the listed applicant for VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2?

The FDA 510(k) record lists Vnus Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2?

The FDA product code for VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 is GEI.

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Other records listing Vnus Medical Technologies, Inc. as applicant

K082890VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 K061373VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 K052003VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40)K033547VNUS VESSEL AND TISSUE COAGULATION SYSTEM K030557MODIFICATION TO VNUS CLOSURE SYSTEM K003092MODIFICATION TO VNUS CLOSURE SYSTEM

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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.