Nk Biotechnical Engineering Co.
Nk Biotechnical Engineering Co. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 1994.
Top product codes for Nk Biotechnical Engineering Co.
Recent clearances by Nk Biotechnical Engineering Co.
- K934368 — NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001
- K923964 — NK GRASP SENSOR, MODEL GA001
- K923965 — NK GRASP SENSOR, MODEL GA002
- K923963 — NK DIGI-GRIP SENSOR, MODEL DGR001
- K921266 — NK MEDICAL MICROMETER, MODEL MC001
- K921268 — NK DYNA-GRIP SENSOR, MODEL DG001
- K914054 — NK GRASP SENSOR, MODEL GR001
- K914055 — PINCH SENSOR, MODEL PF001
- K914056 — NK PINCH SENSOR, MODEL PF002
- K914057 — NK PINCH SENSOR, MODEL PA001
- K914059 — NK DEVIATION SENSOR, MODEL DV001
- K914060 — RANGE OF MOTION SENSOR, MODEL RM001
- K914061 — NK RANGE OF MOTION SENSOR, MODEL RM002
- K914062 — NK DEXTERITLY BOARD, MODEL BX001
- K914058 — NK PINCH SENSOR, MODEL PA002
Data sourced from openFDA. This site is unofficial and independent of the FDA.