Hytek Medical, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Hytek Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Northridge, US.
Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Hytek Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
1 devices