510(k) K123605 ยท HCA Catheter, Ventricular
SMARTFLOW CATHETER
| Applicant | Mri Interventions, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 16, 2013 |
| Received | Nov 21, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123605
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.