510(k) K082412 ยท DTP Defoamer, Cardiopulmonary Bypass
VENOUS BUBBLE TRAP, MODEL VBT 160; VENOUS BUBBLE TRAP WITH BIOLINE COATING, MODEL BE-VBT 160, BEQ-VBT 160
| Applicant | Mapquet Cardiopulmonary AG, Hirrlingen, DE |
| Decision | Substantially Equivalent, Nov 10, 2008 |
| Received | Aug 21, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082412
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.