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FDA 510(k)

Rhino-Laryngo Fiberscope Olympus ENF-GP2

K-Number: K181240 · 2018-10-04

ApplicantOlympus Medical Systems Corp.
Decision Date2018-10-04
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Rhino-Laryngo Fiberscope Olympus ENF-GP2 is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2018-10-04 under approval number K181240. 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 Fiberscope Olympus ENF-GP2?

Rhino-Laryngo Fiberscope Olympus ENF-GP2 is a medical device that received FDA 510(k) clearance on 2018-10-04. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K181240.

When was Rhino-Laryngo Fiberscope Olympus ENF-GP2 approved by the FDA?

Rhino-Laryngo Fiberscope Olympus ENF-GP2 received FDA 510(k) clearance on 2018-10-04, under approval number K181240.

What company makes Rhino-Laryngo Fiberscope Olympus ENF-GP2?

Rhino-Laryngo Fiberscope Olympus ENF-GP2 is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Rhino-Laryngo Fiberscope Olympus ENF-GP2?

The FDA product code for Rhino-Laryngo Fiberscope Olympus ENF-GP2 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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