510(k) K000830 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CANNULATION TOURNIQUET SET, 2 TUBE OR 5 TUBE
| Applicant | California Medical Laboratories, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 7, 2000 |
| Received | Mar 14, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000830
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.