FDA 510(k)

ARTHROCARE ENT PLASMA WAND

K-Number: K070374 · 2007-04-25

Decision Date2007-04-25

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ARTHROCARE ENT PLASMA WAND is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 2007-04-25 under 510(k) number K070374. 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 ENT PLASMA WAND?

ARTHROCARE ENT PLASMA WAND is a medical device that received FDA 510(k) clearance on 2007-04-25. The listed applicant is Arthrocare Corp.. The 510(k) number is K070374.

When did ARTHROCARE ENT PLASMA WAND receive FDA 510(k) clearance?

ARTHROCARE ENT PLASMA WAND received FDA 510(k) clearance on 2007-04-25, under 510(k) number K070374.

Who is the listed applicant for ARTHROCARE ENT PLASMA WAND?

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 ENT PLASMA WAND?

The FDA product code for ARTHROCARE ENT PLASMA WAND 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.