Zyter, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Zyter, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rockville, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Zyter, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Zyter, Inc.
1 devices