510(k) K051830 ยท GZL Electrode, Depth
NEURODRIVE SYSTEM
| Applicant | Alpha Omega , Ltd., Nazareth Illit, IL |
| Decision | Substantially Equivalent, Sep 16, 2005 |
| Received | Jul 6, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051830
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.