Starfish Product Engineering, Inc. is one of 680 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Starfish Product Engineering, Inc. - FDA 510(k) Cleared Devices
Recent clearances: POD B-SCAN
1
Total
1
Cleared
0
Denied
Starfish Product Engineering, Inc. has 1 FDA 510(k) cleared medical devices. Based in Victoria, B.C.,, CA.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Starfish Product Engineering, Inc. 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 - Starfish Product Engineering, Inc.
1 devices