XVbeam2000
K-Number: K233914 · 2024-02-08
Decision Date2024-02-08
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
XVbeam2000 is a medical device manufactured by Shenzhen Xpectvision Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-02-08 under approval number K233914. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the XVbeam2000?
XVbeam2000 is a medical device that received FDA 510(k) clearance on 2024-02-08. It is manufactured by Shenzhen Xpectvision Technology Co., Ltd.. The 510(k) number is K233914.
When was XVbeam2000 approved by the FDA?
XVbeam2000 received FDA 510(k) clearance on 2024-02-08, under approval number K233914.
What company makes XVbeam2000?
XVbeam2000 is manufactured by Shenzhen Xpectvision Technology Co., Ltd..
What is the FDA product code for XVbeam2000?
The FDA product code for XVbeam2000 is EHD.
Other Devices by Shenzhen Xpectvision Technology Co., Ltd.
Related Devices (Code: EHD)
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.