510(k) K992208 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM
| Applicant | Ge Medical Systems, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jul 12, 1999 |
| Received | Jun 30, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992208
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.