510(k) K012560 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
GE LOGIQ A100 MP, MODEL 2272413
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Aug 23, 2001 |
| Received | Aug 8, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012560
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.