510(k) K111384 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
LIFEBRIDGE
| Applicant | Lifebridge Medizintechnik AG, Fairfield IA, US |
| Decision | Substantially Equivalent, May 24, 2011 |
| Received | May 17, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K111384
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.