Nk Biotechnical Engineering Co. - FDA 510(k) Cleared Devices
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.
15 devices
Cleared
Aug 11, 1994
NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001
Neurology
338d
Cleared
May 12, 1993
NK GRASP SENSOR, MODEL GA001
Neurology
278d
Cleared
May 12, 1993
NK GRASP SENSOR, MODEL GA002
Neurology
278d
Cleared
Mar 31, 1993
NK DIGI-GRIP SENSOR, MODEL DGR001
Neurology
236d
Cleared
Jul 14, 1992
NK MEDICAL MICROMETER, MODEL MC001
Orthopedic
120d
Cleared
Jul 14, 1992
NK DYNA-GRIP SENSOR, MODEL DG001
Neurology
120d
Cleared
Dec 09, 1991
NK GRASP SENSOR, MODEL GR001
Neurology
90d
Cleared
Dec 09, 1991
PINCH SENSOR, MODEL PF001
Neurology
90d
Cleared
Dec 09, 1991
NK PINCH SENSOR, MODEL PF002
Neurology
90d
Cleared
Dec 09, 1991
NK PINCH SENSOR, MODEL PA001
Neurology
90d
Cleared
Dec 09, 1991
NK DEVIATION SENSOR, MODEL DV001
Neurology
90d
Cleared
Dec 09, 1991
RANGE OF MOTION SENSOR, MODEL RM001
Neurology
90d