Zyter, Inc. is one of 19009 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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