# Nk Biotechnical Engineering Co.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 15 (1991–1994): 15 510(k) clearances
- Product codes: LBB (10), KQX (3), KTZ (1), LLN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K934368: NK Pressure-Specified Sensory Device, Model PSSD-001 (Aug 11, 1994)
- K923965: NK Grasp Sensor, Model GA002 (May 12, 1993)
- K923964: NK Grasp Sensor, Model GA001 (May 12, 1993)
- K923963: NK Digi-Grip Sensor, Model DGR001 (Mar 31, 1993)
- K921266: NK Medical Micrometer, Model MC001 (Jul 14, 1992)
- K921268: NK Dyna-Grip Sensor, Model DG001 (Jul 14, 1992)
- K914055: Pinch Sensor, Model PF001 (Dec 9, 1991)
- K914062: NK Dexteritly Board, Model BX001 (Dec 9, 1991)

Source page: https://510kreport.com/company/nk-biotechnical-engineering