Prodigm, Inc. is one of 25391 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Prodigm, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chico, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Prodigm, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Prodigm, Inc.
1 devices