510(k) K991611 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
GE LOGIQ 500
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jun 9, 1999 |
| Received | May 10, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991611
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.