510(k) K840948 ยท GKX Instrument, Automated Platelet Counting
CLEAR POROUS PLASTIC-HYPOALLERGENIC
| Applicant | Gainor Medical MD, US |
| Decision | Substantially Equivalent, Aug 14, 1984 |
| Received | Jul 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840948
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.