510(k) K840749 ยท DTY Sensor, Blood-Gas, In-Line, Cardiopulmonary Bypass
GAST STAT MONITORING SYSTEM
| Applicant | Cardiovascular Devices, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Apr 17, 1984 |
| Received | Feb 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840749
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.