510(k) K843486 ยท LLN Device, Vibration Threshold Measurement
VIBRAMETER
| Applicant | Somedic AB, Sweden, US |
| Decision | Substantially Equivalent, Dec 24, 1984 |
| Received | Sep 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843486
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.