Knox Medical Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Knox Medical Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Aluna
1
Total
1
Cleared
0
Denied
Knox Medical Diagnostics, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Knox Medical Diagnostics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies as regulatory consultant.
FDA 510(k) Regulatory Record - Knox Medical Diagnostics, Inc.
1 devices