510(k) K840134 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
CAMTEX 1000
| Applicant | Digital Imaging Co. of America, Walker MI, US |
| Decision | Substantially Equivalent, Mar 16, 1984 |
| Received | Jan 4, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840134
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.