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FDA 510(k)

ENTEC PLASMA WANDS

K-Number: K014290 · 2002-03-28

ApplicantArthrocare Corp.
Decision Date2002-03-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENTEC PLASMA 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 2002-03-28 under 510(k) number K014290. 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 ENTEC PLASMA WANDS?

ENTEC PLASMA WANDS is a medical device that received FDA 510(k) clearance on 2002-03-28. The listed applicant is Arthrocare Corp.. The 510(k) number is K014290.

When did ENTEC PLASMA WANDS receive FDA 510(k) clearance?

ENTEC PLASMA WANDS received FDA 510(k) clearance on 2002-03-28, under 510(k) number K014290.

Who is the listed applicant for ENTEC PLASMA 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 ENTEC PLASMA WANDS?

The FDA product code for ENTEC PLASMA 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.

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