Airway Mobilescope
K-Number: K201300 · 2021-01-26
ApplicantOlympus Medical Systems Corp.
Decision Date2021-01-26
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent
Device Summary
Airway Mobilescope is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2021-01-26 under approval number K201300. 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 Airway Mobilescope?
Airway Mobilescope is a medical device that received FDA 510(k) clearance on 2021-01-26. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K201300.
When was Airway Mobilescope approved by the FDA?
Airway Mobilescope received FDA 510(k) clearance on 2021-01-26, under approval number K201300.
What company makes Airway Mobilescope?
Airway Mobilescope is manufactured by Olympus Medical Systems Corp..
What is the FDA product code for Airway Mobilescope?
The FDA product code for Airway Mobilescope is EOQ.
Other Devices by Olympus Medical Systems Corp.
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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.