510(k) K860806 ยท DXF Catheter, Septostomy
REGULATED PRESSURE INJECTOR
| Applicant | Target Therapeutics, Los Angeles CA, US |
| Decision | Substantially Equivalent, Mar 31, 1986 |
| Received | Mar 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860806
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.