XVbeam2000
K-Number: K233914 · 2024-02-08
Device Summary
Frequently Asked Questions
What is the XVbeam2000?
XVbeam2000 is a medical device that received FDA 510(k) clearance on 2024-02-08. The listed applicant is Shenzhen Xpectvision Technology Co., Ltd.. The 510(k) number is K233914.
When did XVbeam2000 receive FDA 510(k) clearance?
XVbeam2000 received FDA 510(k) clearance on 2024-02-08, under 510(k) number K233914.
Who is the listed applicant for XVbeam2000?
The FDA 510(k) record lists Shenzhen Xpectvision Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XVbeam2000?
The FDA product code for XVbeam2000 is EHD.
Other records listing Shenzhen Xpectvision Technology Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EHD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.