510(k) K813549 ยท DRS Transducer, Blood-Pressure, Extravascular
CONTINUOUS FLUSH DEVICE
| Applicant | Namic, Walker MI, US |
| Decision | Substantially Equivalent, Jan 12, 1982 |
| Received | Dec 21, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813549
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.