Callisyn Biomedical, Inc. is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Callisyn Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FluidiTube 2.7F Infusion Micro Catheter, 110 cm and 130 cm
1
Total
1
Cleared
0
Denied
Callisyn Biomedical, Inc. has 1 FDA 510(k) cleared medical devices. Based in North Andover, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Callisyn Biomedical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Icon as regulatory consultant.
FDA 510(k) Regulatory Record - Callisyn Biomedical, Inc.
1 devices