510(k) K020789 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
GE VIVID 3 EXPERT; GE VIVID 3 PRO
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Apr 4, 2002 |
| Received | Mar 11, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020789
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.