510(k) K811391 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
OXIMETRIX ACCU SAT CPB
| Applicant | Oximetrix, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 20, 1981 |
| Received | May 18, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811391
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.