510(k) K823558 ยท JPI Device, Hematocrit Measuring
MICRO-HEMATOCRIT CENTRIFUGE 335/336
| Applicant | Fisher Scientific Co., LLC, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 21, 1983 |
| Received | Dec 2, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823558
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.