FDA 510(k)

ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM

K-Number: K961069 · 1996-05-28

Decision Date1996-05-28

Product CodeFAS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ARTHROCARE UROLOGIC MULTI-ELECTRODE 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 1996-05-28 under 510(k) number K961069. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM?

ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM is a medical device that received FDA 510(k) clearance on 1996-05-28. The listed applicant is Arthrocare Corp.. The 510(k) number is K961069.

When did ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM receive FDA 510(k) clearance?

ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM received FDA 510(k) clearance on 1996-05-28, under 510(k) number K961069.

Who is the listed applicant for ARTHROCARE UROLOGIC MULTI-ELECTRODE 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 UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM?

The FDA product code for ARTHROCARE UROLOGIC MULTI-ELECTRODE ELECTROSURGERY SYSTEM is FAS.

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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.