510(k) K022022 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
JOSTRA VENT CATHETERS, MODELS LV & HKV
| Applicant | Jostra AG, Oxford PA, US |
| Decision | Substantially Equivalent, Sep 11, 2002 |
| Received | Jun 20, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022022
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.