510(k) K782036 ยท GYD Transducer, Tremor
TREMOR MONITOR
| Applicant | Columbus Instruments Intl. Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 23, 1979 |
| Received | Dec 5, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782036
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.