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FDA 510(k)

Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3

K-Number: K221638 · 2022-09-19

ApplicantOlympus Medical Systems Corp.
Decision Date2022-09-19
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3 is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2022-09-19 under approval number K221638. 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-VH, Rhino-Laryngo Videoscope Olympus ENF-V3?

Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3 is a medical device that received FDA 510(k) clearance on 2022-09-19. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K221638.

When was Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3 approved by the FDA?

Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3 received FDA 510(k) clearance on 2022-09-19, under approval number K221638.

What company makes Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3?

Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3 is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3?

The FDA product code for Rhino-Laryngo Videoscope Olympus ENF-VH, Rhino-Laryngo Videoscope Olympus ENF-V3 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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