Sandstone Diagnostics, Inc. is one of 13197 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sandstone Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Trak Plus Male Fertility Testing System, Trak Male Fertility Testing System
2
Total
2
Cleared
0
Denied
Sandstone Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Livermore, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Sandstone Diagnostics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ammirati Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Sandstone Diagnostics, Inc.
2 devices