510(k) K853608 ยท LLN Device, Vibration Threshold Measurement
NEUROMETER
| Applicant | Neurotron, Inc., Baltimore MD, US |
| Decision | Substantially Equivalent, Jun 12, 1986 |
| Received | Aug 28, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853608
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.