Nk Biotechnical Engineering Co.
Minneapolis, MN, US
Nk Biotechnical Engineering Co. appears in FDA device records in Minneapolis, MN. FDA records list 15 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 15
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 15 510(k) clearances for Nk Biotechnical Engineering Co. between 1991 and 1994. The busiest year on record is 1991, with 9. The most recent is 1994, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 9 |
| 1992 | 2 |
| 1993 | 3 |
| 1994 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K934368 | NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 | LLN | Substantially Equivalent | |
| K923965 | NK GRASP SENSOR, MODEL GA002 | LBB | Substantially Equivalent | |
| K923964 | NK GRASP SENSOR, MODEL GA001 | LBB | Substantially Equivalent | |
| K923963 | NK DIGI-GRIP SENSOR, MODEL DGR001 | LBB | Substantially Equivalent | |
| K921268 | NK DYNA-GRIP SENSOR, MODEL DG001 | LBB | Substantially Equivalent | |
| K921266 | NK MEDICAL MICROMETER, MODEL MC001 | KTZ | Substantially Equivalent | |
| K914062 | NK DEXTERITLY BOARD, MODEL BX001 | KQX | Substantially Equivalent | |
| K914061 | NK RANGE OF MOTION SENSOR, MODEL RM002 | KQX | Substantially Equivalent | |
| K914060 | RANGE OF MOTION SENSOR, MODEL RM001 | KQX | Substantially Equivalent | |
| K914059 | NK DEVIATION SENSOR, MODEL DV001 | LBB | Substantially Equivalent | |
| K914057 | NK PINCH SENSOR, MODEL PA001 | LBB | Substantially Equivalent | |
| K914056 | NK PINCH SENSOR, MODEL PF002 | LBB | Substantially Equivalent | |
| K914055 | PINCH SENSOR, MODEL PF001 | LBB | Substantially Equivalent | |
| K914054 | NK GRASP SENSOR, MODEL GR001 | LBB | Substantially Equivalent | |
| K914058 | NK PINCH SENSOR, MODEL PA002 | LBB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain