510(k) K950153 ยท FPA Set, Administration, Intravascular
VENTED/NONVENTED GEMINI ADMINISTRATION SET WITH CHECK VALVE AND TWO SAFSITE(TM) VALVES
| Applicant | Imed Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 24, 1995 |
| Received | Jan 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950153
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.