510(k) K040531 ยท FMI Needle, Hypodermic, Single Lumen
TERUMO SURGUARD2 SAFETY NEEDLE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Mar 23, 2004 |
| Received | Mar 1, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040531
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.