Cardiowise, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiowise, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SQuEEZ Software
1
Total
1
Cleared
0
Denied
Cardiowise, Inc. has 1 FDA 510(k) cleared medical devices. Based in Fayetteville, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cardiowise, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cardiowise, Inc.
1 devices