510(k) K910679 ยท GKL Counter, Cell, Automated (Particle Counter)
GENESIS I AUTOMATED CELL COUNTER
| Applicant | Alicia Diagnostics, Inc., Oviedo FL, US |
| Decision | Substantially Equivalent, May 7, 1991 |
| Received | Feb 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910679
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.