510(k) K001763 ยท MQS System, Hemodialysis, Access Recirculation Monitoring
CRIT-LINE MONITOR III (CLM III)
| Applicant | In-Line Diagnostics Corp., Kaysville UT, US |
| Decision | Substantially Equivalent, Dec 20, 2000 |
| Received | Jun 12, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001763
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.