510(k) K912341 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
MULTICAM I 8X10
| Applicant | Camtronics, Ltd., Hartland WI, US |
| Decision | Substantially Equivalent, Aug 26, 1991 |
| Received | May 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912341
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.