XiniWave II Model ECS322P
K-Number: K171092 · 2017-07-10
ApplicantInternational Trade Group, Inc.
Decision Date2017-07-10
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
XiniWave II Model ECS322P is a medical device manufactured by International Trade Group, Inc.. It received FDA 510(k) clearance on 2017-07-10 under approval number K171092. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the XiniWave II Model ECS322P?
XiniWave II Model ECS322P is a medical device that received FDA 510(k) clearance on 2017-07-10. It is manufactured by International Trade Group, Inc.. The 510(k) number is K171092.
When was XiniWave II Model ECS322P approved by the FDA?
XiniWave II Model ECS322P received FDA 510(k) clearance on 2017-07-10, under approval number K171092.
What company makes XiniWave II Model ECS322P?
XiniWave II Model ECS322P is manufactured by International Trade Group, Inc..
What is the FDA product code for XiniWave II Model ECS322P?
The FDA product code for XiniWave II Model ECS322P is NGX.
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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.