510(k) K050126 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
GE LOGIQ TWIN
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Feb 2, 2005 |
| Received | Jan 19, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050126
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.