510(k) K781680 ยท DRS Transducer, Blood-Pressure, Extravascular
MONITORING, PRESSURE KIT
| Applicant | Pharmaseal Div., Baxter Healthcare Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 6, 1978 |
| Received | Oct 2, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781680
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.