510(k) K875251 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ARTIS 3200 DIAGNOSTIC ULTRASOUND DEVICE
| Applicant | Philips Medical Systems (Cleveland), Inc., Highland Heights OH, US |
| Decision | Substantially Equivalent, May 11, 1988 |
| Received | Dec 22, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875251
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.