FDA 510(k)

ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM

K-Number: K010568 · 2001-03-27

Decision Date2001-03-27

Product CodeKNS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 2001-03-27 under 510(k) number K010568. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM?

ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM is a medical device that received FDA 510(k) clearance on 2001-03-27. The listed applicant is Arthrocare Corp.. The 510(k) number is K010568.

When did ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM receive FDA 510(k) clearance?

ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM received FDA 510(k) clearance on 2001-03-27, under 510(k) number K010568.

Who is the listed applicant for ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM?

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 UROLOGY ELECTROSURGERY SYSTEM?

The FDA product code for ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM is KNS.

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Related Devices (Code: KNS)

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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.