510(k) K130280 ยท DTZ Oxygenator, Cardiopulmonary Bypass
CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR
| Applicant | Terumo Corporation, Elkton MD, US |
| Decision | Substantially Equivalent, Mar 13, 2013 |
| Received | Feb 5, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130280
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.