510(k) K911113 ยท ITX Transducer, Ultrasonic, Diagnostic
INTERSON TRANSRECTAL PROBE/KONTRON ULTRASOUND SYST
| Applicant | Interson Corp., San Leandro CA, US |
| Decision | Substantially Equivalent, Dec 17, 1991 |
| Received | Mar 7, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911113
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.