510(k) K171580
K171580 is an FDA 510(k) premarket notification submitted by Ge Medical Systems (China) Co., Ltd. for the device "Monitor B125, Monitor B105". The FDA issued a decision of Substantially Equivalent on Nov 1, 2017. The device falls under product code MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)), a Class II device regulated under 21 CFR 870.1025.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 1, 2017
- Date Received
- May 31, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- Device Class
- Class II
- Regulation Number
- 870.1025
- Review Panel
- CV
- Submission Type
- 510(k)