Spencer Technologies is one of 21643 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spencer Technologies - FDA 510(k) Cleared Devices
Recent clearances: PMD VIEWER, TCD 100M, PWD13 TRANSDUCER
2
Total
2
Cleared
0
Denied
Spencer Technologies has 2 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 2 cleared submissions from 2000 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Spencer Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Spencer Technologies
2 devices