510(k) K854423 ยท LIB Device, General Purpose, Microbiology, Diagnostic
IMMULON 1 EIA TUBES, IMMULON 2 EIA TUBES
| Applicant | Dynatech Laboratories, Inc., Alexandria VA, US |
| Decision | Substantially Equivalent, Nov 20, 1985 |
| Received | Nov 5, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854423
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.