510(k) K833171 ยท DRS Transducer, Blood-Pressure, Extravascular
MONITORING KIT
| Applicant | Transamerica Delaval, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Sep 6, 1984 |
| Received | Sep 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833171
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.