Medical Device Manufacturer · US , Mchenry , IL

Kantron Cardiovascular, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1981

Total

Cleared

Denied

Kantron Cardiovascular, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1981 to 1981. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Kantron Cardiovascular, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kantron Cardiovascular, Inc.

2 devices

1-2 of 2