Medical Depot is one of 18363 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Depot - FDA 510(k) Cleared Devices
Recent clearances: DRIVE SOLSTICE OXYGEN CONCENTRATOR
1
Total
1
Cleared
0
Denied
Medical Depot has 1 FDA 510(k) cleared medical devices. Based in Apollo Beach, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medical Depot Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Medical Depot
1 devices