510(k) K050265 ยท JOZ System, Automated Platelet Aggregation
CHRONO-LOG WHOLE BLOOD LUMI-AGGREGOMETER, MODEL 700
| Applicant | Chrono-Log Corp., Havertown PA, US |
| Decision | Substantially Equivalent, Oct 14, 2005 |
| Received | Feb 4, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050265
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.