510(k) K072075 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
MODIFICATION TO GE LOGIQ A3
| Applicant | General Electric Co., Wauwatosa WI, US |
| Decision | Substantially Equivalent, Aug 29, 2007 |
| Received | Jul 30, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072075
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.