510(k) K870967 ยท ITX Transducer, Ultrasonic, Diagnostic
ADMS TRANSRECTAL 7.5 MHZ PROBE
| Applicant | Diasonics, Inc., Milipitas CA, US |
| Decision | Substantially Equivalent, Sep 29, 1987 |
| Received | Mar 10, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870967
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.