510(k) K020351 ยท DTZ Oxygenator, Cardiopulmonary Bypass
D 903 AVANT 2 PH.I.S.I.O. ADULT HOLLOW FIBER OXYGENATOR
| Applicant | Dideco S.P.A., Waltham MA, US |
| Decision | Substantially Equivalent, Feb 26, 2002 |
| Received | Feb 4, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020351
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.