510(k) K770002 ยท DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass
CONSOLE, MOBILE FOR 3 PUMPS W/MASTS
| Applicant | Cobe Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 7, 1977 |
| Received | Jan 3, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770002
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.