510(k) K912249 ยท KPZ Generator, High Voltage, X-Ray, Therapeutic
PATIENT DOSE MONITOR
| Applicant | Theta Systems, Inc., Melbourne FL, US |
| Decision | Substantially Equivalent, Aug 30, 1991 |
| Received | May 21, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912249
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.