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.

15 devices
1–12 of 15
NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001
K934368 · LLN Device, Vibration Threshold Measurement · Neurology
Aug 1994 338d
NK GRASP SENSOR, MODEL GA001
K923964 · LBB Dynamometer, Ac-powered · Neurology
May 1993 278d
NK GRASP SENSOR, MODEL GA002
K923965 · LBB Dynamometer, Ac-powered · Neurology
May 1993 278d
NK DIGI-GRIP SENSOR, MODEL DGR001
K923963 · LBB Dynamometer, Ac-powered · Neurology
Mar 1993 236d
NK MEDICAL MICROMETER, MODEL MC001
K921266 · KTZ Caliper · Orthopedic
Jul 1992 120d
NK DYNA-GRIP SENSOR, MODEL DG001
K921268 · LBB Dynamometer, Ac-powered · Neurology
Jul 1992 120d
NK GRASP SENSOR, MODEL GR001
K914054 · LBB Dynamometer, Ac-powered · Neurology
Dec 1991 90d
PINCH SENSOR, MODEL PF001
K914055 · LBB Dynamometer, Ac-powered · Neurology
Dec 1991 90d
NK PINCH SENSOR, MODEL PF002
K914056 · LBB Dynamometer, Ac-powered · Neurology
Dec 1991 90d
NK PINCH SENSOR, MODEL PA001
K914057 · LBB Dynamometer, Ac-powered · Neurology
Dec 1991 90d
NK DEVIATION SENSOR, MODEL DV001
K914059 · LBB Dynamometer, Ac-powered · Neurology
Dec 1991 90d
RANGE OF MOTION SENSOR, MODEL RM001
K914060 · KQX Goniometer, Ac-powered · Neurology
Dec 1991 90d
Filters