510(k) K110202 ยท ITX Transducer, Ultrasonic, Diagnostic
FUJIFILM DIAGNOSTIC ULTRASOUND SYSTEM FAZONE CB
| Applicant | Fujifilm Medical System U.S.A., Inc., Stamford CT, US |
| Decision | Substantially Equivalent, Feb 8, 2011 |
| Received | Jan 24, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110202
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.