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FDA 510(k)

ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475

K-Number: K024291 · 2003-03-20

ApplicantArthrex, Inc.
Decision Date2003-03-20
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475 is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2003-03-20 under 510(k) number K024291. 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 ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475?

ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475 is a medical device that received FDA 510(k) clearance on 2003-03-20. The listed applicant is Arthrex, Inc.. The 510(k) number is K024291.

When did ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475 receive FDA 510(k) clearance?

ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475 received FDA 510(k) clearance on 2003-03-20, under 510(k) number K024291.

Who is the listed applicant for ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475?

The FDA 510(k) record lists Arthrex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475?

The FDA product code for ARTHREX CONTINUOUS WAVE III ARTHOSCOPY PUMP, MODEL AR-6475 is HRX.

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Related Devices (Code: HRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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