510(k) K800555 ยท DTZ Oxygenator, Cardiopulmonary Bypass
PARTNER SEVEN DISP. BUBBLE OXYGENATOR
| Applicant | Cardiovascular Research, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 4, 1980 |
| Received | Mar 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800555
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.