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FDA 510(k)

ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970

K-Number: K962321 · 1996-07-19

ApplicantArthrocare Corp.
Decision Date1996-07-19
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 is the device name listed in this FDA 510(k) record. The listed applicant is Arthrocare Corp.. It received FDA 510(k) clearance on 1996-07-19 under 510(k) number K962321. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970?

ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 is a medical device that received FDA 510(k) clearance on 1996-07-19. The listed applicant is Arthrocare Corp.. The 510(k) number is K962321.

When did ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 receive FDA 510(k) clearance?

ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 received FDA 510(k) clearance on 1996-07-19, under 510(k) number K962321.

Who is the listed applicant for ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970?

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 ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970?

The FDA product code for ARTHOCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 is HRX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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