FDA 510(k) Submission Follows the Successful Completion of the Pivotal Human Clinical Trial
FDA 510(k) Clearance Anticipated During the Second Quarter of 2025
Read more at globenewswire.comFDA 510(k) Submission Follows the Successful Completion of the Pivotal Human Clinical Trial
FDA 510(k) Clearance Anticipated During the Second Quarter of 2025
Read more at globenewswire.com