510(k) K041027 ยท IZI System, X-Ray, Angiographic
DIGITAL RADIOGRAPHY SYSTEM WITH FLAT PANEL DETECTOR, MODEL DFP8000D
| Applicant | Toshibamedical Systems Corporation, Tustin CA, US |
| Decision | Substantially Equivalent, May 14, 2004 |
| Received | Apr 21, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041027
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.