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FDA 510(k)

KARL STORZ TELESCOPE BRIDGES AND ADAPTERS

K-Number: K946023 · 1994-12-20

Decision Date1994-12-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ TELESCOPE BRIDGES AND ADAPTERS 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 1994-12-20 under 510(k) number K946023. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ TELESCOPE BRIDGES AND ADAPTERS?

KARL STORZ TELESCOPE BRIDGES AND ADAPTERS is a medical device that received FDA 510(k) clearance on 1994-12-20. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K946023.

When did KARL STORZ TELESCOPE BRIDGES AND ADAPTERS receive FDA 510(k) clearance?

KARL STORZ TELESCOPE BRIDGES AND ADAPTERS received FDA 510(k) clearance on 1994-12-20, under 510(k) number K946023.

Who is the listed applicant for KARL STORZ TELESCOPE BRIDGES AND ADAPTERS?

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 KARL STORZ TELESCOPE BRIDGES AND ADAPTERS?

The FDA product code for KARL STORZ TELESCOPE BRIDGES AND ADAPTERS is GCJ.

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: GCJ)

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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