The following data is part of a premarket notification filed by Ge Medical Systems Information Technologies, Inc. with the FDA for Mars Holter Analysis Workstation.
| Device ID | K132437 |
| 510k Number | K132437 |
| Device Name: | MARS HOLTER ANALYSIS WORKSTATION |
| Classification | Computer, Diagnostic, Programmable |
| Applicant | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. 9900 WEST INNOVATION DRIVE Wauwatosa, WI 53226 |
| Contact | Kristin Pabst |
| Correspondent | Kristin Pabst GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. 9900 WEST INNOVATION DRIVE Wauwatosa, WI 53226 |
| Product Code | DQK |
| CFR Regulation Number | 870.1425 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-08-05 |
| Decision Date | 2013-12-04 |
| Summary: | summary |