510(k) K895771 ยท FMI Needle, Hypodermic, Single Lumen
EXEL SPINAL NEEDLES
| Applicant | Exel Intl., Culver City CA, US |
| Decision | Substantially Equivalent, Feb 16, 1990 |
| Received | Sep 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895771
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.