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FDA 510(k)

MEDICAM ARTHROSCOPE SYSTEMS

K-Number: K900812 · 1990-05-03

Decision Date1990-05-03
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MEDICAM ARTHROSCOPE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1990-05-03 under 510(k) number K900812. 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 MEDICAM ARTHROSCOPE SYSTEMS?

MEDICAM ARTHROSCOPE SYSTEMS is a medical device that received FDA 510(k) clearance on 1990-05-03. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K900812.

When did MEDICAM ARTHROSCOPE SYSTEMS receive FDA 510(k) clearance?

MEDICAM ARTHROSCOPE SYSTEMS received FDA 510(k) clearance on 1990-05-03, under 510(k) number K900812.

Who is the listed applicant for MEDICAM ARTHROSCOPE SYSTEMS?

The FDA 510(k) record lists Kirschner Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICAM ARTHROSCOPE SYSTEMS?

The FDA product code for MEDICAM ARTHROSCOPE SYSTEMS is HRX.

Related Clinical Trials

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.

Other records listing Kirschner Medical Corp. as applicant

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.

View all 76 devices →

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.

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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