510(k) K834067 ยท GRO Antisera, Fluorescent, All Types, Hemophilus Spp.
LEGIONELLA DIFFERENTIATION DISK
| Applicant | Remel Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 3, 1984 |
| Received | Nov 25, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834067
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.