The following data is part of a premarket notification filed by Fischer Imaging Corp. with the FDA for Ep-x.
| Device ID | K934481 |
| 510k Number | K934481 |
| Device Name: | EP-X |
| Classification | System, X-ray, Fluoroscopic, Image-intensified |
| Applicant | FISCHER IMAGING CORP. 12300 NORTH GRANT ST. Denver, CO 80241 -3120 |
| Contact | James W Morgan |
| Correspondent | James W Morgan FISCHER IMAGING CORP. 12300 NORTH GRANT ST. Denver, CO 80241 -3120 |
| Product Code | JAA |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-14 |
| Decision Date | 1993-11-03 |