FDA 510(k)

ARTHROCARE ARTHRO WANDS, ENETEC EVAC PLASMA WAND

K-Number: K013463 · 2001-11-15

Decision Date2001-11-15

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ARTHROCARE ARTHRO WANDS, ENETEC EVAC 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 2001-11-15 under 510(k) number K013463. 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 ARTHRO WANDS, ENETEC EVAC PLASMA WAND?

ARTHROCARE ARTHRO WANDS, ENETEC EVAC PLASMA WAND is a medical device that received FDA 510(k) clearance on 2001-11-15. The listed applicant is Arthrocare Corp.. The 510(k) number is K013463.

When did ARTHROCARE ARTHRO WANDS, ENETEC EVAC PLASMA WAND receive FDA 510(k) clearance?

ARTHROCARE ARTHRO WANDS, ENETEC EVAC PLASMA WAND received FDA 510(k) clearance on 2001-11-15, under 510(k) number K013463.

Who is the listed applicant for ARTHROCARE ARTHRO WANDS, ENETEC EVAC 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 ARTHRO WANDS, ENETEC EVAC PLASMA WAND?

The FDA product code for ARTHROCARE ARTHRO WANDS, ENETEC EVAC 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.