510(k) K964205 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
BETTER-TUBING
| Applicant | Circulatory Technology, Inc., Oyster Bay NY, US |
| Decision | Substantially Equivalent, Apr 8, 1998 |
| Received | Oct 18, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964205
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.