510(k) K833705 ยท FMI Needle, Hypodermic, Single Lumen
BETAJECT BD U100
| Applicant | Orange Medical Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 9, 1984 |
| Received | Oct 18, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833705
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.