510(k) K900758 ยท DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line
HEPARINIZED ARTERIAL SCREEN BLOOD FILTER
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, May 17, 1990 |
| Received | Feb 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900758
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.