510(k) K863342 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
SOFTIP CORONARY SINUS CARDIOPLEGIA CATHETER
| Applicant | Angiomedics, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 3, 1987 |
| Received | Aug 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863342
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.