510(k) K900860 ยท DTY Sensor, Blood-Gas, In-Line, Cardiopulmonary Bypass
PERFUSION MONITOR
| Applicant | Cardio Metrics, Inc., Sugar Land TX, US |
| Decision | Substantially Equivalent, Aug 14, 1990 |
| Received | Feb 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900860
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.