6420 Ultrasound System
K-Number: K183191 · 2018-12-04
ApplicantEsaote, S.p.A.
Decision Date2018-12-04
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
6420 Ultrasound System is a medical device manufactured by Esaote, S.p.A.. It received FDA 510(k) clearance on 2018-12-04 under approval number K183191. 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 6420 Ultrasound System?
6420 Ultrasound System is a medical device that received FDA 510(k) clearance on 2018-12-04. It is manufactured by Esaote, S.p.A.. The 510(k) number is K183191.
When was 6420 Ultrasound System approved by the FDA?
6420 Ultrasound System received FDA 510(k) clearance on 2018-12-04, under approval number K183191.
What company makes 6420 Ultrasound System?
6420 Ultrasound System is manufactured by Esaote, S.p.A..
What is the FDA product code for 6420 Ultrasound System?
The FDA product code for 6420 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.