510(k) K983551 ยท GKF Instrument, Hematocrit, Automated
CRIT-SCAN II MONITOR
| Applicant | In-Line Diagnostics Corp., Farmington UT, US |
| Decision | Substantially Equivalent, May 27, 1999 |
| Received | Oct 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983551
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.