510(k) K924331 ยท LIO Device, Specimen Collection
TRANSYSTEM LIQUID STUART MEDIUM
| Applicant | Pro-Lab Diagnostics, Ontario, CA |
| Decision | Substantially Equivalent, Dec 24, 1992 |
| Received | Aug 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924331
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.