510(k) K123178 ยท GXI Probe, Radiofrequency Lesion
STRYKER VENOM ELECTRODES AND CANNULAE
| Applicant | Stryker Instruments, Instruments Div., Kalamazoo MI, US |
| Decision | Substantially Equivalent, Mar 28, 2013 |
| Received | Oct 9, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123178
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.