510(k) K000387 ยท FMI Needle, Hypodermic, Single Lumen
TERUMO NEEDLE WITH LOCKING SHEATH
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Mar 2, 2000 |
| Received | Feb 7, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K000387
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.