510(k) K014073 ยท FMF Syringe, Piston
HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE
| Applicant | Portex, Inc., Keene NH, US |
| Decision | Substantially Equivalent, Feb 13, 2002 |
| Received | Dec 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014073
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.