510(k) K790546 ยท DTX Gas Control Unit, Cardiopulmonary Bypass
FLOWMETER, OPTIFLO GAS
| Applicant | Cobe Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 11, 1979 |
| Received | Mar 20, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790546
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.