Shepherd Scientific, Inc. is one of 24544 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shepherd Scientific, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DOCKING STATION,TEIRSTEIN EDGE,ANGIOASSIST COMBINATION DEVICE, ANGIOASSIST FAMILY
1
Total
1
Cleared
0
Denied
Shepherd Scientific, Inc. has 1 FDA 510(k) cleared medical devices. Based in La Jolla, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Shepherd Scientific, 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 - Shepherd Scientific, Inc.
1 devices