510(k) K883412 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
THE CARPENTIER TRANS-MITRAL VENTRICULAR VENT(TM)
| Applicant | Promedica Products, Inc., Newport Beach CA, US |
| Decision | Substantially Equivalent, Feb 8, 1989 |
| Received | Aug 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883412
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.