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FDA 510(k)

EVIS EXERA III Bronchovideoscope Olympus BF-XT190

K-Number: K183419 · 2019-09-05

ApplicantOlympus Medical Systems Corp.
Decision Date2019-09-05
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EVIS EXERA III Bronchovideoscope Olympus BF-XT190 is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2019-09-05 under approval number K183419. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVIS EXERA III Bronchovideoscope Olympus BF-XT190?

EVIS EXERA III Bronchovideoscope Olympus BF-XT190 is a medical device that received FDA 510(k) clearance on 2019-09-05. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K183419.

When was EVIS EXERA III Bronchovideoscope Olympus BF-XT190 approved by the FDA?

EVIS EXERA III Bronchovideoscope Olympus BF-XT190 received FDA 510(k) clearance on 2019-09-05, under approval number K183419.

What company makes EVIS EXERA III Bronchovideoscope Olympus BF-XT190?

EVIS EXERA III Bronchovideoscope Olympus BF-XT190 is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for EVIS EXERA III Bronchovideoscope Olympus BF-XT190?

The FDA product code for EVIS EXERA III Bronchovideoscope Olympus BF-XT190 is EOQ.

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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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