Nuclear Cardiology Systems, Inc. is one of 25165 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nuclear Cardiology Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CARDIOSPECT D90/CARDIO CAM, NEUROSPECTQUAD GAMMA CAMERA
2
Total
2
Cleared
0
Denied
Nuclear Cardiology Systems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 2 cleared submissions from 2002 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Nuclear Cardiology Systems, 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 - Nuclear Cardiology Systems, Inc.
2 devices