510(k) K071785 ยท FMI Needle, Hypodermic, Single Lumen
HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE, HYPODERMIC NEEDLE-PRO EDGE SAFETY DEVICE WITH SYRINGE
| Applicant | Smiths Medical Asd, Inc., Keene NH, US |
| Decision | Substantially Equivalent, Aug 2, 2007 |
| Received | Jul 2, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K071785
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.