510(k) K822000 ยท DTY Sensor, Blood-Gas, In-Line, Cardiopulmonary Bypass
EXTRACORPOREAL BLOOD GAS SYSTEM
| Applicant | Cardiovascular Devices, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 22, 1982 |
| Received | Jul 7, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822000
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.