510(k) K822821 ยท DTW Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass
GAMBRO BLOOD LEVEL DETECTOR LCS 10
| Applicant | Gambro, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Oct 18, 1982 |
| Received | Sep 20, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822821
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.