Oncology Data Systems, Inc. is one of 20446 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oncology Data Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MUCHECK, VERSION 9.0, MUCHECK V8, MUCHECK V7.0
4
Total
4
Cleared
0
Denied
Oncology Data Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.
Historical record: 4 cleared submissions from 2001 to 2010. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Oncology Data Systems, 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 - Oncology Data Systems, Inc.
4 devices