510(k) K082185 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2
| Applicant | Ge Medical Systems Ultrasound and Primary Care Dia, Wauwatosa WI, US |
| Decision | Substantially Equivalent, Aug 15, 2008 |
| Received | Aug 1, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082185
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 22, 2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL GE LOGIQ E9 ultrasound system
Product Usage:
The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); N Terminated |
IYO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.