510(k) K990288 ยท FPA Set, Administration, Intravascular
FREE FLOW SAFETY DEVICE, MODEL MG 245052
| Applicant | Teva Medical, Ltd., Englewood Cliffs NJ, US |
| Decision | Substantially Equivalent, Feb 24, 1999 |
| Received | Jan 29, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990288
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.