510(k) K950942 ยท JPI Device, Hematocrit Measuring
CRIT-LINE HEMATOCRIT ALERT
| Applicant | In-Line Diagnostics Corp., Riverdale UT, US |
| Decision | Substantially Equivalent, Mar 14, 1995 |
| Received | Feb 15, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950942
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.