510(k) K032135 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
SITE-RITE IV ULTRASOUND SYSTEM
| Applicant | Dymax Corp, Pittsburgh PA, US |
| Decision | Substantially Equivalent, Jul 21, 2003 |
| Received | Jul 11, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032135
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.