510(k) K894412 ยท LMA Digitizer, Image, Radiological
RADIOSCOPE OR MAMMOSCOPE
| Applicant | Vision Ten, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Dec 22, 1989 |
| Received | Jul 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894412
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.