510(k) K904198 ยท FMI Needle, Hypodermic, Single Lumen
SAFETY NEEDLE SHEATH
| Applicant | Concord/Portex, Keene NH, US |
| Decision | Substantially Equivalent, Dec 19, 1990 |
| Received | Sep 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904198
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.