510(k) K161342 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
Sonic Window
| Applicant | Analogic Corporation, Peabody MA, US |
| Decision | Substantially Equivalent, Jun 15, 2016 |
| Received | May 13, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161342
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.