X-View 3D Pan/X-View 2D Pan
K-Number: K222666 · 2023-07-10
Device Summary
Frequently Asked Questions
What is the X-View 3D Pan/X-View 2D Pan?
X-View 3D Pan/X-View 2D Pan is a medical device that received FDA 510(k) clearance on 2023-07-10. The listed applicant is Trident S.R.L. The 510(k) number is K222666.
When did X-View 3D Pan/X-View 2D Pan receive FDA 510(k) clearance?
X-View 3D Pan/X-View 2D Pan received FDA 510(k) clearance on 2023-07-10, under 510(k) number K222666.
Who is the listed applicant for X-View 3D Pan/X-View 2D Pan?
The FDA 510(k) record lists Trident S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-View 3D Pan/X-View 2D Pan?
The FDA product code for X-View 3D Pan/X-View 2D Pan is OAS.
Other records listing Trident S.R.L 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: OAS)
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.