510(k) K895359 ยท ITX Transducer, Ultrasonic, Diagnostic
ADMS MULTIPLANE RECTAL PROBE
| Applicant | Avalon Technology Corp., Indianapolis IN, US |
| Decision | Substantially Equivalent, Nov 22, 1989 |
| Received | Aug 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895359
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.