510(k) K081921 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
GE VIVID E9 ULTRASOUND
| Applicant | General Electric Co., Wauwatosa WI, US |
| Decision | Substantially Equivalent, Aug 6, 2008 |
| Received | Jul 7, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081921
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.