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FDA 510(k)

THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM

K-Number: K881014 · 1988-04-14

Decision Date1988-04-14
Product CodeFWF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM 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 1988-04-14 under 510(k) number K881014. 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 THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM?

THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K881014.

When did THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM receive FDA 510(k) clearance?

THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM received FDA 510(k) clearance on 1988-04-14, under 510(k) number K881014.

Who is the listed applicant for THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM?

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 MINI 9000 SOLID STATE CCD VIDEO CAM?

The FDA product code for THE KARL STORZ MINI 9000 SOLID STATE CCD VIDEO CAM 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 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: 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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