510(k) K884792 ยท FMI Needle, Hypodermic, Single Lumen
VASCULAR ACCESS PORT HUBER POINT INFUSION NEEDLES
| Applicant | Infucare Products, Inc., Tarpon Springs FL, US |
| Decision | Substantially Equivalent, Jan 30, 1989 |
| Received | Nov 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884792
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.