FDA 510(k)

VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100

K-Number: K061373 · 2006-08-01

ApplicantVnus Medical Technologies, Inc.

Decision Date2006-08-01

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 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 2006-08-01 under 510(k) number K061373. 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 CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100?

VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 is a medical device that received FDA 510(k) clearance on 2006-08-01. The listed applicant is Vnus Medical Technologies, Inc.. The 510(k) number is K061373.

When did VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 receive FDA 510(k) clearance?

VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 received FDA 510(k) clearance on 2006-08-01, under 510(k) number K061373.

Who is the listed applicant for VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100?

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 CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100?

The FDA product code for VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 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 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 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.