XBody Go USA, XBody Pro USA
K-Number: K221200 · 2023-01-31
ApplicantXbody Hungary Kft.
Decision Date2023-01-31
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
XBody Go USA, XBody Pro USA is a medical device manufactured by Xbody Hungary Kft.. It received FDA 510(k) clearance on 2023-01-31 under approval number K221200. 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 XBody Go USA, XBody Pro USA?
XBody Go USA, XBody Pro USA is a medical device that received FDA 510(k) clearance on 2023-01-31. It is manufactured by Xbody Hungary Kft.. The 510(k) number is K221200.
When was XBody Go USA, XBody Pro USA approved by the FDA?
XBody Go USA, XBody Pro USA received FDA 510(k) clearance on 2023-01-31, under approval number K221200.
What company makes XBody Go USA, XBody Pro USA?
XBody Go USA, XBody Pro USA is manufactured by Xbody Hungary Kft..
What is the FDA product code for XBody Go USA, XBody Pro USA?
The FDA product code for XBody Go USA, XBody Pro USA 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.