510(k) K882034 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
INTRA-ART(TM) INTERNAL MAMMARY INFUSION CATHETER
| Applicant | Buckman Co., Inc., Martinez CA, US |
| Decision | Substantially Equivalent, Jul 28, 1988 |
| Received | May 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882034
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.