510(k) K972470 ยท MQS System, Hemodialysis, Access Recirculation Monitoring
CRIT-LINE MONITOR (CLMIII)
| Applicant | In-Line Diagnostics Corp., Great Neck NY, US |
| Decision | Substantially Equivalent, Dec 11, 1997 |
| Received | Jul 1, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972470
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.