510(k) K843444 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
ARGYLE SILICONE LEFT VENTRICULAR AND
| Applicant | Sherwood Medical Co., St. Louis MS, US |
| Decision | Substantially Equivalent, Oct 18, 1984 |
| Received | Sep 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843444
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.