510(k) K002248 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
DINAMAP PRO 1000 MONITOR, MODEL 1000
| Applicant | Critikon Company, LLC, Tampa FL, US |
| Decision | Substantially Equivalent, Sep 21, 2000 |
| Received | Jul 25, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002248
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.