510(k) K900227 ยท LMD System, Digital Image Communications, Radiological
MVP (MULTI-VENDOR PROTOCOL CONVERTOR)
| Applicant | Merge Technologies, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Feb 12, 1990 |
| Received | Jan 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900227
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 28, 2006 | Konica Minolta Medical Imaging USA, Inc. Konica Minolta PrintLink III Model - ID/IV, code no. 0770, 0771 Medical Imaging Communication Device
Model IV - product code 5000230
Model ID, product code 5000330
Konica Minolta Medical & Graphi Terminated |
LMD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.