510(k) K013608 ยท OWB Interventional Fluoroscopic X-Ray System
DIGITAL RADIOGRAPHY SYSTEM, MODEL DFP-8000D
| Applicant | Toshiba America Medical Systems, In.C, Tustin CA, US |
| Decision | Substantially Equivalent, Nov 15, 2001 |
| Received | Oct 31, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013608
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 23, 2006 | Toshiba American Med Sys Inc Toshiba Digital Radiography System Model DFP8000D Terminated |
JAA | None listed |
| Aug 11, 2004 | Toshiba American Med Sys Inc Digital Radiography System, model DFP-8000D Terminated |
JAA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.