510(k) K082798 ยท KPR System, X-Ray, Stationary
DIGITAL DIAGNOSTIC X-RAY SYSTEM, MODELS MAK 1500, MAK 2000 AND MAK 3000
| Applicant | Medicatech USA, Deer Field IL, US |
| Decision | Substantially Equivalent, Oct 28, 2008 |
| Received | Sep 23, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082798
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.