510(k) K955232 ยท LMB Device, Digital Image Storage, Radiological
NT SERIES DIGITAL IMAGE MANAGER
| Applicant | Camtronics, Ltd., Hartland WI, US |
| Decision | Substantially Equivalent, Dec 11, 1995 |
| Received | Nov 14, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955232
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.