510(k) K982412 ยท MQS System, Hemodialysis, Access Recirculation Monitoring
MODIFICATION OF CRIT-LINE MONITOR III (CLM III)
| Applicant | In-Line Diagnostics Corp., Farmington UT, US |
| Decision | Substantially Equivalent, Oct 9, 1998 |
| Received | Jul 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982412
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.