510(k) K911114 ยท ITX Transducer, Ultrasonic, Diagnostic
INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEM
| Applicant | Interson Corp., San Leandro CA, US |
| Decision | Substantially Equivalent, Nov 19, 1991 |
| Received | Mar 7, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911114
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.