510(k) K093371 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
MODEL DGH 6000 SCANMATE A
| Applicant | Dgh Technology, Inc., Exton PA, US |
| Decision | Substantially Equivalent, Apr 5, 2010 |
| Received | Oct 29, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093371
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.