510(k) K001965 ยท FMI Needle, Hypodermic, Single Lumen
SAFE-POINT VAC, SAFE-POINT M-D BLOOD COLLECTION SYSTEMS
| Applicant | North American Medical Products, Inc., Albany NY, US |
| Decision | Substantially Equivalent, Feb 2, 2001 |
| Received | Jun 28, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001965
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.