510(k) K073188 ยท FMI Needle, Hypodermic, Single Lumen
HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE
| Applicant | Smiths Medical Asd, Inc., Keene NH, US |
| Decision | Substantially Equivalent, Feb 8, 2008 |
| Received | Nov 13, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K073188
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.