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FDA 510(k)

VISERA RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V

K-Number: K021073 · 2002-05-01

ApplicantOlympus America, Inc.
Decision Date2002-05-01
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VISERA RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V 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 2002-05-01 under 510(k) number K021073. 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 RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V?

VISERA RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V is a medical device that received FDA 510(k) clearance on 2002-05-01. The listed applicant is Olympus America, Inc.. The 510(k) number is K021073.

When did VISERA RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V receive FDA 510(k) clearance?

VISERA RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V received FDA 510(k) clearance on 2002-05-01, under 510(k) number K021073.

Who is the listed applicant for VISERA RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V?

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 RHINLARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V?

The FDA product code for VISERA RHINLARYNGOVIDEOSCOPE 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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