FDA 510(k)

VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2

K-Number: K082890 · 2008-10-15

ApplicantVnus Medical Technologies, Inc.

Decision Date2008-10-15

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 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 2008-10-15 under 510(k) number K082890. 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 INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2?

VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 is a medical device that received FDA 510(k) clearance on 2008-10-15. The listed applicant is Vnus Medical Technologies, Inc.. The 510(k) number is K082890.

When did VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 receive FDA 510(k) clearance?

VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 received FDA 510(k) clearance on 2008-10-15, under 510(k) number K082890.

Who is the listed applicant for VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2?

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 INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2?

The FDA product code for VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 is GEI.

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Other records listing Vnus Medical Technologies, Inc. as applicant

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 K003092MODIFICATION 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.