Broncho Videoscope System
K-Number: K231521 · 2023-11-14
ApplicantScivita Medical Technology Co., Ltd.
Decision Date2023-11-14
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent
Device Summary
Broncho Videoscope System is a medical device manufactured by Scivita Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-11-14 under approval number K231521. 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 Broncho Videoscope System?
Broncho Videoscope System is a medical device that received FDA 510(k) clearance on 2023-11-14. It is manufactured by Scivita Medical Technology Co., Ltd.. The 510(k) number is K231521.
When was Broncho Videoscope System approved by the FDA?
Broncho Videoscope System received FDA 510(k) clearance on 2023-11-14, under approval number K231521.
What company makes Broncho Videoscope System?
Broncho Videoscope System is manufactured by Scivita Medical Technology Co., Ltd..
What is the FDA product code for Broncho Videoscope System?
The FDA product code for Broncho Videoscope System 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.