510(k) K031453 ยท FMI Needle, Hypodermic, Single Lumen
TERUMO SURGUARD 2 SAFETY NEEDLE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Jul 8, 2003 |
| Received | May 7, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031453
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.