510(k) K171301 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
Scanmate Flex
| Applicant | Dgh Technology, Inc., Exton PA, US |
| Decision | Substantially Equivalent, Jul 31, 2017 |
| Received | May 3, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171301
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.