510(k) K881028 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
7.5 MHZ ENDORECTAL PROBE
| Applicant | Philips Ultrasound, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Apr 27, 1988 |
| Received | Mar 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881028
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.