510(k) K851271 ยท GRO Antisera, Fluorescent, All Types, Hemophilus Spp.
LEGIONELLA CULTURE CONFIRMATIN KIT
| Applicant | Gen-Probe, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jul 8, 1985 |
| Received | Apr 1, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851271
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.