510(k) K843935 ยท LIO Device, Specimen Collection
MODIFICATION MICROTRAK DIRECT SPECIMEN TEST
| Applicant | Syva Co., Palo Alto CA, US |
| Decision | Substantially Equivalent, Oct 23, 1984 |
| Received | Oct 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843935
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.