Cardiogard Medical, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiogard Medical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CardioGard Emboli Protection Cannula
2
Total
2
Cleared
0
Denied
Cardiogard Medical, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Amherst, US.
Historical record: 2 cleared submissions from 2015 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiogard Medical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cardiogard Medical, Ltd.
2 devices