510(k) K860076 ยท DTW Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass
GAMBRO ULTRASONIC BLOOD LEVEL DETECTOR ULD 10-200
| Applicant | Gambro, Inc., Lincolnshire IL, US |
| Decision | Substantially Equivalent, May 30, 1986 |
| Received | Jan 8, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860076
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.