FDA 510(k)

VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V

K-Number: K022445 · 2003-01-24

Decision Date2003-01-24

Product CodeHIH

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Optical Co., Ltd.. It received FDA 510(k) clearance on 2003-01-24 under 510(k) number K022445. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V?

VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V is a medical device that received FDA 510(k) clearance on 2003-01-24. The listed applicant is Olympus Optical Co., Ltd.. The 510(k) number is K022445.

When did VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V receive FDA 510(k) clearance?

VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V received FDA 510(k) clearance on 2003-01-24, under 510(k) number K022445.

Who is the listed applicant for VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V?

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

What is the FDA product code for VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V?

The FDA product code for VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V is HIH.

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Other records listing Olympus Optical Co., Ltd. as applicant

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Related Devices (Code: HIH)

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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.