Navi e/Navi s/Navi X Diagnostic Ultrasound System
K-Number: K180461 · 2018-05-09
Decision Date2018-05-09
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Navi e/Navi s/Navi X Diagnostic Ultrasound System is a medical device manufactured by Shenzhen Wisonic Medical Technology Co. , Ltd.. It received FDA 510(k) clearance on 2018-05-09 under approval number K180461. 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 Navi e/Navi s/Navi X Diagnostic Ultrasound System?
Navi e/Navi s/Navi X Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2018-05-09. It is manufactured by Shenzhen Wisonic Medical Technology Co. , Ltd.. The 510(k) number is K180461.
When was Navi e/Navi s/Navi X Diagnostic Ultrasound System approved by the FDA?
Navi e/Navi s/Navi X Diagnostic Ultrasound System received FDA 510(k) clearance on 2018-05-09, under approval number K180461.
What company makes Navi e/Navi s/Navi X Diagnostic Ultrasound System?
Navi e/Navi s/Navi X Diagnostic Ultrasound System is manufactured by Shenzhen Wisonic Medical Technology Co. , Ltd..
What is the FDA product code for Navi e/Navi s/Navi X Diagnostic Ultrasound System?
The FDA product code for Navi e/Navi s/Navi X Diagnostic 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.