FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Mural Clinical Viewer
K Number: K222586
·
Decision Dec 21, 2022
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
424
Applicant Total
31
Review Days
117
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Basic Information
- Device Name
- Mural Clinical Viewer
- K Number
- K222586
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1025
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ge Medical Systems Information Technologies, Inc.
- Date Received
- August 26, 2022
- Decision Date
- December 21, 2022
- Product Code
- MHX
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MHX | Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | FDA class 2 | Cardiovascular |
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| K231870 | CASE V7.0 Cardiac Testing System and CardioSoft V7.0 Cardiac Testing System | Dec 13, 2023 | Substantially Equivalent |
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| K230145 | ONE-CUF | Mar 14, 2023 | Substantially Equivalent |
| K221904 | EK12 V2 Algorithm | Dec 20, 2022 | Substantially Equivalent |
| K221321 | MAC 5 A4/ MAC 5 A5/ MAC 5 Lite Resting ECG Analysis System | Oct 18, 2022 | Substantially Equivalent |