510(k) K953519 ยท GKF Instrument, Hematocrit, Automated
MICROSPIN 24
| Applicant | Vulcon Technologies, Grandview MO, US |
| Decision | Substantially Equivalent, Nov 3, 1995 |
| Received | Jul 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953519
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.