Knox Medical Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Knox Medical Diagnostics - FDA 510(k) Cleared Devices
Recent clearances: Aluna 2
1
Total
1
Cleared
0
Denied
Knox Medical Diagnostics has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Knox Medical Diagnostics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - Knox Medical Diagnostics
1 devices