510(k) K821159 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
IN-LINE OXYGEN MONITORING SYSTEM
| Applicant | G.D. Searle and Co., Walker MI, US |
| Decision | Substantially Equivalent, May 25, 1982 |
| Received | Apr 22, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821159
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.