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FDA 510(k)

THE KARL STORZ ARTHROPUMP

K-Number: K942298 · 1995-01-17

Decision Date1995-01-17
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE KARL STORZ ARTHROPUMP is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1995-01-17 under 510(k) number K942298. 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 THE KARL STORZ ARTHROPUMP?

THE KARL STORZ ARTHROPUMP is a medical device that received FDA 510(k) clearance on 1995-01-17. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K942298.

When did THE KARL STORZ ARTHROPUMP receive FDA 510(k) clearance?

THE KARL STORZ ARTHROPUMP received FDA 510(k) clearance on 1995-01-17, under 510(k) number K942298.

Who is the listed applicant for THE KARL STORZ ARTHROPUMP?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE KARL STORZ ARTHROPUMP?

The FDA product code for THE KARL STORZ ARTHROPUMP 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 KARL STORZ Endoscopy-America, Inc. 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 355 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

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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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