510(k) K801108 ยท FMI Needle, Hypodermic, Single Lumen
DOUBLE ENDED VENTED TRANSFER DEVICE
| Applicant | Burron Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 30, 1980 |
| Received | May 9, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801108
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.