510(k) K113690 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
GE LOGIQ I, LOGIQ E AND VIVID E
| Applicant | GE Healthcare, Wauwatosa WI, US |
| Decision | Substantially Equivalent, Dec 29, 2011 |
| Received | Dec 15, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113690
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 1, 2013 | GE Healthcare, LLC GE Healthcare, LOGIQ e Ultrasound System.
The LOGIQ i/e and Vivid e is a general purpose ultrasound system intended for use by a qualified physician for evaluation by ultrasound imaging or fluid flo Terminated |
IYN | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.