510(k) K884720 ยท JXC Kit, Screening, Yeast
GERM TUBE SOLUTION
| Applicant | Remel Co., Lenexa KS, US |
| Decision | Substantially Equivalent, Jun 2, 1989 |
| Received | Nov 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884720
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.