510(k) K781984 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
COLLIMATOR, HEART CONTOUR
| Applicant | Siemens Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 4, 1978 |
| Received | Nov 24, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781984
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.