510(k) K922799 ยท DTZ Oxygenator, Cardiopulmonary Bypass
CAPIOX SX HOLLOW FIBER OXYGENATOR
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Sep 2, 1993 |
| Received | Jun 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922799
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.