Cardio-Optics, Inc. is one of 25242 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardio-Optics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEM, CORONARY SINUS ACCESS KIT, MODEL KCS8F-01
2
Total
2
Cleared
0
Denied
Cardio-Optics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 2 cleared submissions from 2005 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardio-Optics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardio-Optics, Inc.
2 devices