Hytek Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hytek Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: sOLVe Tube
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.
FDA 510(k) Regulatory Record - Hytek Medical, Inc.
1 devices