510(k) K971318 ยท GYD Transducer, Tremor
MM-1 MOVEMENT MONITOR
| Applicant | Axon Instruments, Inc., Foster City CA, US |
| Decision | Substantially Equivalent, Jul 28, 1997 |
| Received | Apr 9, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971318
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.