Medical Device Manufacturer · US , Mchenry , IL

Burdick Corp. - FDA 510(k) Cleared Devices

38 submissions · 38 cleared · Since 1976
38
Total
38
Cleared
0
Denied

Burdick Corp. has 38 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.

Historical record: 38 cleared submissions from 1976 to 1994.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Burdick Corp.
38 devices
1-12 of 38

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