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FDA 510(k)

KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM

K-Number: K990154 · 1999-06-01

Decision Date1999-06-01
Product CodeFWF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Imaging, Inc.. It received FDA 510(k) clearance on 1999-06-01 under 510(k) number K990154. The device is classified under product code FWF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM?

KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM is a medical device that received FDA 510(k) clearance on 1999-06-01. The listed applicant is Karl Storz Imaging, Inc.. The 510(k) number is K990154.

When did KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM receive FDA 510(k) clearance?

KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM received FDA 510(k) clearance on 1999-06-01, under 510(k) number K990154.

Who is the listed applicant for KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM?

The FDA 510(k) record lists Karl Storz Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM?

The FDA product code for KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM is FWF.

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 Imaging, 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 10 devices →

Related Devices (Code: FWF)

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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