Medical Device Manufacturer · US , Minneapolis , MN

Nk Biotechnical Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997
2
Total
2
Cleared
0
Denied

Nk Biotechnical Corp. has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 2 cleared submissions from 1997 to 1998. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Nk Biotechnical Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Nk Biotechnical Corp.

2 devices
1-2 of 2
Cleared Jul 17, 1998
DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002
K981730 · LBB
Neurology · 63d
Cleared May 02, 1997
DIGIT-GRIP WITH LCD (DGR002)
K970870 · HRW
Neurology · 53d
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