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Nk Biotechnical Engineering Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K934368NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001August 11, 1994
K923964NK GRASP SENSOR, MODEL GA001May 12, 1993
K923965NK GRASP SENSOR, MODEL GA002May 12, 1993
K923963NK DIGI-GRIP SENSOR, MODEL DGR001March 31, 1993
K921266NK MEDICAL MICROMETER, MODEL MC001July 14, 1992
K921268NK DYNA-GRIP SENSOR, MODEL DG001July 14, 1992
K914054NK GRASP SENSOR, MODEL GR001December 9, 1991
K914059NK DEVIATION SENSOR, MODEL DV001December 9, 1991
K914062NK DEXTERITLY BOARD, MODEL BX001December 9, 1991
K914055PINCH SENSOR, MODEL PF001December 9, 1991
K914060RANGE OF MOTION SENSOR, MODEL RM001December 9, 1991
K914061NK RANGE OF MOTION SENSOR, MODEL RM002December 9, 1991
K914056NK PINCH SENSOR, MODEL PF002December 9, 1991
K914057NK PINCH SENSOR, MODEL PA001December 9, 1991
K914058NK PINCH SENSOR, MODEL PA002December 6, 1991