510(k) K831225 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
GAS-STAT MONITORING SYSTEM
| Applicant | Cardiovascular Devices, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 27, 1983 |
| Received | Apr 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831225
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.