510(k) K961207 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
EP-X BIPLANE
| Applicant | Fischer Imaging Corp., Denver CO, US |
| Decision | Substantially Equivalent, Aug 20, 1996 |
| Received | Mar 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961207
| 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.