Medical Device Manufacturer · US , Minneapolis , MN

Nk Biotechnical Engineering Co. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1991
15
Total
15
Cleared
0
Denied

Nk Biotechnical Engineering Co. has 15 FDA 510(k) cleared neurology devices. Based in Minneapolis, US.

Historical record: 15 cleared submissions from 1991 to 1994.

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

FDA 510(k) Regulatory Record - Nk Biotechnical Engineering Co.
15 devices
1-15 of 15
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