510(k) K970943 ยท GZL Electrode, Depth
GUIDELINE SYSTEM
| Applicant | Axon Instruments, Inc., Foster City CA, US |
| Decision | Substantially Equivalent, Aug 18, 1997 |
| Received | Mar 14, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970943
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.