Medical Device Manufacturer · US , North Andover , MA

Callisyn Biomedical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Total

Cleared

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.

Callisyn Biomedical, Inc. is one of 4735 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Callisyn Biomedical, Inc.

1 devices

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