FDA 510(k)

ARTHROCARE WANDS

K-Number: K060823 · 2006-04-10

Decision Date2006-04-10

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ARTHROCARE WANDS is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 2006-04-10 under 510(k) number K060823. 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 ARTHROCARE WANDS?

ARTHROCARE WANDS is a medical device that received FDA 510(k) clearance on 2006-04-10. The listed applicant is Arthrocare Corp.. The 510(k) number is K060823.

When did ARTHROCARE WANDS receive FDA 510(k) clearance?

ARTHROCARE WANDS received FDA 510(k) clearance on 2006-04-10, under 510(k) number K060823.

Who is the listed applicant for ARTHROCARE WANDS?

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 ARTHROCARE WANDS?

The FDA product code for ARTHROCARE WANDS 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.