510(k) K093832 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass
LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES
| Applicant | Levitronix, LLC, Waltham MA, US |
| Decision | Substantially Equivalent, Jan 13, 2010 |
| Received | Dec 14, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093832
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.