510(k) K103357 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
LIFEBRIDGE
| Applicant | Lifebridge Medizintechnik AG, Bryn Mawr PA, US |
| Decision | Substantially Equivalent, Dec 27, 2010 |
| Received | Nov 16, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103357
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.