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FDA 510(k)

RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP

K-Number: K221660 · 2022-12-28

ApplicantOlympus Medical Systems Corp.
Decision Date2022-12-28
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2022-12-28 under approval number K221660. 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-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP?

RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP is a medical device that received FDA 510(k) clearance on 2022-12-28. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K221660.

When was RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP approved by the FDA?

RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP received FDA 510(k) clearance on 2022-12-28, under approval number K221660.

What company makes RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP?

RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP?

The FDA product code for RHINO-LARYNGOFIBERSCOPE OLYMPUS ENF TYPE-XP 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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