510(k) K890532 ยท ITX Transducer, Ultrasonic, Diagnostic
EUP-C321 5.0MHZ CONVEX TYPE PROBE
| Applicant | Hitachi Medical Corp. of America, Tarrytown NY, US |
| Decision | Substantially Equivalent, Apr 13, 1990 |
| Received | Feb 2, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890532
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.