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FDA 510(k)

ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES

K-Number: K992621 · 1999-11-08

ApplicantAdvanced Diagnostics & Interventions
Decision Date1999-11-08
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Diagnostics & Interventions. It received FDA 510(k) clearance on 1999-11-08 under 510(k) number K992621. 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 ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES?

ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1999-11-08. The listed applicant is Advanced Diagnostics & Interventions. The 510(k) number is K992621.

When did ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES receive FDA 510(k) clearance?

ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES received FDA 510(k) clearance on 1999-11-08, under 510(k) number K992621.

Who is the listed applicant for ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES?

The FDA 510(k) record lists Advanced Diagnostics & Interventions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES?

The FDA product code for ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES is HRX.

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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.

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