510(k) K902631 ยท DTN Reservoir, Blood, Cardiopulmonary Bypass
COBE ICU CONVERSION KIT
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Dec 17, 1990 |
| Received | Jun 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902631
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.