510(k) K152161 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Thoratec CentriMag Return (Arterial) Cannula Kit
| Applicant | Thoratec Corporation, Pleasanton CA, US |
| Decision | Substantially Equivalent, Sep 18, 2015 |
| Received | Aug 3, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152161
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.