510(k) K792202 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
TROCAR CATHETER/THORACIC CATHETER
| Applicant | Portex, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 20, 1979 |
| Received | Nov 2, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792202
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.