510(k) K062342 ยท DRS Transducer, Blood-Pressure, Extravascular
TRUEPULSE DISPOSABLE INVASIVE BLOOD PRESSURE MONITORING KIT
| Applicant | Sentra Medical Devices, LLC, Canton MI, US |
| Decision | Substantially Equivalent, Sep 25, 2006 |
| Received | Aug 11, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062342
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.