510(k) K890351 ยท IZF System, X-Ray, Tomographic
ORTHORALIX SD/ORTHORALIX SD CEPH
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jun 15, 1989 |
| Received | Jan 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890351
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.