510(k) K953875 ยท MQS System, Hemodialysis, Access Recirculation Monitoring
CRIT-LINE HEMATOCRIT ALERT (MODIFICATION)
| Applicant | In-Line Diagnostics Corp., Riverdale UT, US |
| Decision | Substantially Equivalent, Jul 23, 1996 |
| Received | Jun 28, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953875
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.