510(k) K843709 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
COBE SATURATION CELL
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Oct 24, 1984 |
| Received | Sep 21, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843709
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.