510(k) K992227 ยท MQS System, Hemodialysis, Access Recirculation Monitoring
CRIT-LINE MONITOR III (CLM III)
| Applicant | In-Line Diagnostics Corp., Farmington UT, US |
| Decision | Substantially Equivalent, Jul 30, 1999 |
| Received | Jul 2, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992227
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.