510(k) K930478 ยท LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems
READAR
| Applicant | Alamar Biosciences, Inc., Sacramento CA, US |
| Decision | Substantially Equivalent, Oct 22, 1993 |
| Received | Jan 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930478
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.