510(k) K010981 ยท LLN Device, Vibration Threshold Measurement
GSA GENITO SENSORY ANALYZER
| Applicant | Medoc Ltd. Advanced Medical Systems, Minnetonka MN, US |
| Decision | Substantially Equivalent, Sep 20, 2001 |
| Received | Apr 2, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010981
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.