510(k) K934368 ยท LLN Device, Vibration Threshold Measurement
NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001
| Applicant | Nk Biotechnical Engineering Co., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 11, 1994 |
| Received | Sep 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934368
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.