The following data is part of a premarket notification filed by Marquette Electronics, Inc. with the FDA for Eagle 3000/3100 Patient Monitor.
| Device ID | K960272 |
| 510k Number | K960272 |
| Device Name: | EAGLE 3000/3100 PATIENT MONITOR |
| Classification | Monitor, St Segment With Alarm |
| Applicant | MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Contact | Dianne Schmitz |
| Correspondent | Dianne Schmitz MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. Milwaukee, WI 53223 |
| Product Code | MLD |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-18 |
| Decision Date | 1996-10-02 |
| Summary: | summary |