510(k) K895352 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
KENDALL INFANT ECMO VENOVENOUS CATHETER-DUAL LUMEN
| Applicant | Kendall Healthcare Products Co. Div.Of Tyco Health, Mansfield MA, US |
| Decision | Substantially Equivalent, Nov 29, 1989 |
| Received | Sep 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895352
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.