510(k) K020263 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
LOGIQ 3
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Feb 6, 2002 |
| Received | Jan 25, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020263
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 12, 2008 | GE Healthcare Clinical Systems GE LOGIQ 3 Expert ultrasound scanner with software versions 4.0.5, 4.1.1 and 4.1.2. GE Healthcare P.O. Box 414, Milwaukee, Wisconsin 53201 Terminated |
IYN | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.