510(k) K010478 ยท DTZ Oxygenator, Cardiopulmonary Bypass
DIDECO D901 LILLIPUT HOLLOW FIBER OXYGENATOR WITH OR WITHOUT SOFT VENOUS RESERVOIR BAG, WITH BIOCOMPATABLE TREATMENT SUR
| Applicant | Dideco, Arvada CO, US |
| Decision | Substantially Equivalent, Sep 27, 2001 |
| Received | Feb 20, 2001 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K010478
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.