510(k) K870748 ยท ITX Transducer, Ultrasonic, Diagnostic
7.5 MHZ TRANSRECTAL (ENDORECTAL) PROBE
| Applicant | Philips Ultrasound, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Apr 10, 1987 |
| Received | Feb 25, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870748
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.