510(k) K980906 ยท MQS System, Hemodialysis, Access Recirculation Monitoring
TRANSONIC HEMODIALYSIS MONITOR, CARDIAC OUTPUT, MODEL HD01-CO
| Applicant | Transonic Systems, Inc., Ithaca NY, US |
| Decision | Substantially Equivalent, Oct 6, 1998 |
| Received | Mar 10, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980906
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.