510(k) K802423 ยท GRO Antisera, Fluorescent, All Types, Hemophilus Spp.
PHADEBACT HAEMOPHILUS TEST
| Applicant | Pharmacia, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 12, 1980 |
| Received | Oct 3, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802423
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.