510(k) K103469 ยท KRL Detector, Bubble, Cardiopulmonary Bypass
STOCKERT AIR PURGE CONTROL SYSTEM MODEL 23-45-05
| Applicant | Sorin Group Deutschland GmbH, North Attleboro MA, US |
| Decision | Substantially Equivalent, Jan 18, 2011 |
| Received | Nov 24, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103469
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.