510(k) K913914 ยท FMI Needle, Hypodermic, Single Lumen
PROGUARDII(TM) BLOOD COLLECTION DEVICE
| Applicant | Care Medical Devices, Inc., Ontario CA, US |
| Decision | Substantially Equivalent, Oct 8, 1991 |
| Received | Sep 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913914
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.