FDA 510(k)

MODIFICATION TO VNUS CLOSURE SYSTEM

K-Number: K003092 · 2000-12-18

ApplicantVnus Medical Technologies, Inc.

Decision Date2000-12-18

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO VNUS CLOSURE SYSTEM 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 2000-12-18 under 510(k) number K003092. 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 MODIFICATION TO VNUS CLOSURE SYSTEM?

MODIFICATION TO VNUS CLOSURE SYSTEM is a medical device that received FDA 510(k) clearance on 2000-12-18. The listed applicant is Vnus Medical Technologies, Inc.. The 510(k) number is K003092.

When did MODIFICATION TO VNUS CLOSURE SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO VNUS CLOSURE SYSTEM received FDA 510(k) clearance on 2000-12-18, under 510(k) number K003092.

Who is the listed applicant for MODIFICATION TO VNUS CLOSURE SYSTEM?

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 MODIFICATION TO VNUS CLOSURE SYSTEM?

The FDA product code for MODIFICATION TO VNUS CLOSURE SYSTEM 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)K040638VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 K033547VNUS VESSEL AND TISSUE COAGULATION SYSTEM K030557MODIFICATION TO VNUS CLOSURE SYSTEM

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.