510(k) K881758 ยท FMI Needle, Hypodermic, Single Lumen
VIGGO VASCUPORT NEEDLE
| Applicant | Ohmeda Medical, Tampa FL, US |
| Decision | Substantially Equivalent, Jun 3, 1988 |
| Received | Apr 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881758
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.