510(k) K874037 ยท DQO Catheter, Intravascular, Diagnostic
ANGIO WASTE FLUIDS DUMP BAG
| Applicant | Procedure Products, Inc., Vancouver WA, US |
| Decision | Substantially Equivalent, Jan 29, 1988 |
| Received | Oct 5, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874037
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.