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FDA 510(k)

Rhino-Laryngo Videoscope Olympus ENF-VT3

K-Number: K183416 · 2019-09-06

ApplicantOlympus Medical Systems Corp.
Decision Date2019-09-06
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Rhino-Laryngo Videoscope Olympus ENF-VT3 is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2019-09-06 under approval number K183416. 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 Rhino-Laryngo Videoscope Olympus ENF-VT3?

Rhino-Laryngo Videoscope Olympus ENF-VT3 is a medical device that received FDA 510(k) clearance on 2019-09-06. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K183416.

When was Rhino-Laryngo Videoscope Olympus ENF-VT3 approved by the FDA?

Rhino-Laryngo Videoscope Olympus ENF-VT3 received FDA 510(k) clearance on 2019-09-06, under approval number K183416.

What company makes Rhino-Laryngo Videoscope Olympus ENF-VT3?

Rhino-Laryngo Videoscope Olympus ENF-VT3 is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Rhino-Laryngo Videoscope Olympus ENF-VT3?

The FDA product code for Rhino-Laryngo Videoscope Olympus ENF-VT3 is EOB.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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