510(k) K904295 ยท FMI Needle, Hypodermic, Single Lumen
PROGUARD(TM) BLOOD COLLECTION NEEDLE
| Applicant | Safety-Ject, Inc., Rancho Cucamonga CA, US |
| Decision | Substantially Equivalent, Oct 15, 1990 |
| Received | Sep 19, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904295
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.