Interson USB Ultrasound System
K-Number: K233734 · 2023-12-22
ApplicantInterson Corporation
Decision Date2023-12-22
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Interson USB Ultrasound System is a medical device manufactured by Interson Corporation. It received FDA 510(k) clearance on 2023-12-22 under approval number K233734. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Interson USB Ultrasound System?
Interson USB Ultrasound System is a medical device that received FDA 510(k) clearance on 2023-12-22. It is manufactured by Interson Corporation. The 510(k) number is K233734.
When was Interson USB Ultrasound System approved by the FDA?
Interson USB Ultrasound System received FDA 510(k) clearance on 2023-12-22, under approval number K233734.
What company makes Interson USB Ultrasound System?
Interson USB Ultrasound System is manufactured by Interson Corporation.
What is the FDA product code for Interson USB Ultrasound System?
The FDA product code for Interson USB Ultrasound System is IYN.
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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.