510(k) K903490 ยท FMI Needle, Hypodermic, Single Lumen
NORPLANT(R) TROCAR
| Applicant | Wyeth-Ayerst Laboratories, Inc., Philadelphia PA, US |
| Decision | Substantially Equivalent, Nov 28, 1990 |
| Received | Jul 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903490
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.