510(k) K884264 ยท FPA Set, Administration, Intravascular
HIGH RISK NEEDLE CONNECTOR ASSEMBLY
| Applicant | Venture Molded Products, Inc., Ewing Township NJ, US |
| Decision | Substantially Equivalent, Nov 14, 1988 |
| Received | Oct 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884264
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.