510(k) K122341 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
PROSOUND F37 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL: PROSOUND F37
| Applicant | Hitachi Aloka Medical, Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, Sep 26, 2012 |
| Received | Aug 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122341
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.