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FDA 510(k)

SOVIS OPTIQUE'S ENDOSCOPIC CABLE

K-Number: K023633 · 2002-12-31

ApplicantSovis Optique
Decision Date2002-12-31
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SOVIS OPTIQUE'S ENDOSCOPIC CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Sovis Optique. It received FDA 510(k) clearance on 2002-12-31 under 510(k) number K023633. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOVIS OPTIQUE'S ENDOSCOPIC CABLE?

SOVIS OPTIQUE'S ENDOSCOPIC CABLE is a medical device that received FDA 510(k) clearance on 2002-12-31. The listed applicant is Sovis Optique. The 510(k) number is K023633.

When did SOVIS OPTIQUE'S ENDOSCOPIC CABLE receive FDA 510(k) clearance?

SOVIS OPTIQUE'S ENDOSCOPIC CABLE received FDA 510(k) clearance on 2002-12-31, under 510(k) number K023633.

Who is the listed applicant for SOVIS OPTIQUE'S ENDOSCOPIC CABLE?

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

What is the FDA product code for SOVIS OPTIQUE'S ENDOSCOPIC CABLE?

The FDA product code for SOVIS OPTIQUE'S ENDOSCOPIC CABLE is FFS.

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.

Related Devices (Code: FFS)

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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