FDA 510(k)

VISAGE COSMETIC SURGERY, MODEL V5000

K-Number: K992180 · 2000-03-20

Decision Date2000-03-20

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VISAGE COSMETIC SURGERY, MODEL V5000 is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 2000-03-20 under 510(k) number K992180. 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 VISAGE COSMETIC SURGERY, MODEL V5000?

VISAGE COSMETIC SURGERY, MODEL V5000 is a medical device that received FDA 510(k) clearance on 2000-03-20. The listed applicant is Arthrocare Corp.. The 510(k) number is K992180.

When did VISAGE COSMETIC SURGERY, MODEL V5000 receive FDA 510(k) clearance?

VISAGE COSMETIC SURGERY, MODEL V5000 received FDA 510(k) clearance on 2000-03-20, under 510(k) number K992180.

Who is the listed applicant for VISAGE COSMETIC SURGERY, MODEL V5000?

The FDA 510(k) record lists Arthrocare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISAGE COSMETIC SURGERY, MODEL V5000?

The FDA product code for VISAGE COSMETIC SURGERY, MODEL V5000 is GEI.

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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.