510(k) K885228 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
RT6800 ECHOCARDIOGRAPHY SYSTEM
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Mar 14, 1989 |
| Received | Dec 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885228
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.