510(k) K934481 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
EP-X
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, Nov 3, 1993 |
| Received | Sep 14, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934481
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 9, 2005 | Fischer Imaging Corporation Electrophysiology Imaging System Terminated |
JAA | None listed |
| Sep 9, 2005 | Fischer Imaging Corporation Electrophysiology Imaging System Terminated |
JAA | None listed |
| Sep 9, 2005 | Fischer Imaging Corporation Electrophysiology Imaging System Terminated |
JAA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.