510(k) K874922 ยท ITX Transducer, Ultrasonic, Diagnostic
ACUSON TRANSPERINEAL NEEDLE GUIDE
| Applicant | Acuson Computed Sonography, Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 19, 1988 |
| Received | Dec 3, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874922
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.