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FDA 510(k)

VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V

K-Number: K031648 · 2003-07-24

ApplicantOlympus Optical Co., Ltd.
Decision Date2003-07-24
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF 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 2003-07-24 under 510(k) number K031648. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V?

VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V is a medical device that received FDA 510(k) clearance on 2003-07-24. The listed applicant is Olympus Optical Co., Ltd.. The 510(k) number is K031648.

When did VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V receive FDA 510(k) clearance?

VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V received FDA 510(k) clearance on 2003-07-24, under 510(k) number K031648.

Who is the listed applicant for VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF 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 RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V?

The FDA product code for VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V is EOB.

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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.

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