510(k) K130636 ยท LMA Digitizer, Image, Radiological
TELERADPRO EDGE; TELERADPRO EDGE HD-CCD
| Applicant | Vidar Systems Corp., Herndon VA, US |
| Decision | Substantially Equivalent, Jun 7, 2013 |
| Received | Mar 11, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130636
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.