510(k) K984322 ยท DTP Defoamer, Cardiopulmonary Bypass
DIDECO D920, LILLIPUT 1 TWIN RESERVOIR
| Applicant | Dideco S.P.A., Waltham MA, US |
| Decision | Substantially Equivalent, Mar 2, 1999 |
| Received | Dec 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984322
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.