510(k) K910421 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
SATURATION/HEMATOCRIT MONITOR SYSTEM
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Oct 15, 1991 |
| Received | Jan 30, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910421
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.