510(k) K090773 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
CFI ULTRASOUND PROBE DRAPE
| Applicant | Contour Fabricators, Inc., Fenton MI, US |
| Decision | Substantially Equivalent, Sep 18, 2009 |
| Received | Mar 23, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090773
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.