The following data is part of a premarket notification filed by General Electric Medical Systems Information Techn with the FDA for Ge Marquette Clinical Information Center, Ge Marquette Cic.
| Device ID | K001112 |
| 510k Number | K001112 |
| Device Name: | GE MARQUETTE CLINICAL INFORMATION CENTER, GE MARQUETTE CIC |
| Classification | Display, Cathode-ray Tube, Medical |
| Applicant | GENERAL ELECTRIC MEDICAL SYSTEMS INFORMATION TECHN 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Contact | David Wahlig |
| Correspondent | David Wahlig GENERAL ELECTRIC MEDICAL SYSTEMS INFORMATION TECHN 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Product Code | DXJ |
| CFR Regulation Number | 870.2450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-04-06 |
| Decision Date | 2000-06-14 |