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FDA 510(k)

ARTHROSCOPES & ASSOCIATED INSTRUMENTS

K-Number: K821359 · 1982-05-27

ApplicantDowns Surgical , Ltd.
Decision Date1982-05-27
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPES & ASSOCIATED INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1982-05-27 under 510(k) number K821359. 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 ARTHROSCOPES & ASSOCIATED INSTRUMENTS?

ARTHROSCOPES & ASSOCIATED INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1982-05-27. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K821359.

When did ARTHROSCOPES & ASSOCIATED INSTRUMENTS receive FDA 510(k) clearance?

ARTHROSCOPES & ASSOCIATED INSTRUMENTS received FDA 510(k) clearance on 1982-05-27, under 510(k) number K821359.

Who is the listed applicant for ARTHROSCOPES & ASSOCIATED INSTRUMENTS?

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

What is the FDA product code for ARTHROSCOPES & ASSOCIATED INSTRUMENTS?

The FDA product code for ARTHROSCOPES & ASSOCIATED INSTRUMENTS 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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