Airway Mobilescope
K-Number: K201300 · 2021-01-26
Device Summary
Frequently Asked Questions
What is the Airway Mobilescope?
Airway Mobilescope is a medical device that received FDA 510(k) clearance on 2021-01-26. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K201300.
When did Airway Mobilescope receive FDA 510(k) clearance?
Airway Mobilescope received FDA 510(k) clearance on 2021-01-26, under 510(k) number K201300.
Who is the listed applicant for Airway Mobilescope?
The FDA 510(k) record lists Olympus Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Airway Mobilescope?
The FDA product code for Airway Mobilescope is EOQ.
Other records listing Olympus Medical Systems Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EOQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.