510(k) K012646 ยท FMI Needle, Hypodermic, Single Lumen
TERUMO 30 GAUGE HYPODERMIC NEEDLE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Aug 27, 2001 |
| Received | Aug 13, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012646
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.