510(k) K181314
IntelliVue Patient Monitor MX100, IntelliVue Multi-Measurement Module X3, IntelliVue Microstream Extension by
Philips Medizin Systeme Boeblingen GmbH
— Product Code MHX
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 4, 2018
- Date Received
- May 17, 2018
- 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