FDA 510(k)

VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA

K-Number: K021074 · 2002-05-02

Decision Date2002-05-02

Product CodeFAJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America, Inc.. It received FDA 510(k) clearance on 2002-05-02 under 510(k) number K021074. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA?

VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA is a medical device that received FDA 510(k) clearance on 2002-05-02. The listed applicant is Olympus America, Inc.. The 510(k) number is K021074.

When did VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA receive FDA 510(k) clearance?

VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA received FDA 510(k) clearance on 2002-05-02, under 510(k) number K021074.

Who is the listed applicant for VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA?

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

What is the FDA product code for VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA?

The FDA product code for VISERA CYSTOVIDEOSCOPE OLYMPUS CYF TYPE V/VA is FAJ.

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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.