Biodrain Medical, Inc. is one of 24892 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biodrain Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIODRAIN STREAMWAY FLUID MANAGEMENT SYSTEM
1
Total
1
Cleared
0
Denied
Biodrain Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mendota Heights, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biodrain Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Biodrain Medical, Inc.
1 devices