510(k) K904587 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
DENSICOMP 250
| Applicant | L. Keroack Co., Canada H3x 3p3, CA |
| Decision | Substantially Equivalent, Jan 24, 1991 |
| Received | Oct 9, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904587
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.