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FDA 510(k)

VNUS CLOSURE SYSTEM

K-Number: K982816 · 1999-03-17

ApplicantVnus Medical Technologies, Inc.
Decision Date1999-03-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

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 1999-03-17 under 510(k) number K982816. 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 CLOSURE SYSTEM?

VNUS CLOSURE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-03-17. The listed applicant is Vnus Medical Technologies, Inc.. The 510(k) number is K982816.

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

VNUS CLOSURE SYSTEM received FDA 510(k) clearance on 1999-03-17, under 510(k) number K982816.

Who is the listed applicant for 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 VNUS CLOSURE SYSTEM?

The FDA product code for VNUS CLOSURE SYSTEM is GEI.

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Other records listing Vnus Medical Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K082890VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2K061373VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100K052003VNUS 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 RFG2K033547VNUS VESSEL AND TISSUE COAGULATION SYSTEMK030557MODIFICATION TO VNUS CLOSURE SYSTEM

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Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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