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FDA 510(k), K103646, INTELLIVUE MX40 PATIENT MONITOR
FDA 510(k), K103646, INTELLIVUE MX40 PATIENT MONITOR
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510(K) Number: K103646
Device Name: INTELLIVUE MX40 PATIENT MONITOR
Manufacturer: PHILLIPS MEDICAL SYSTEMS
Device Classification Name: monitor, physiological, patient(with arrhythmia detection or alarms)
Regulation Number: 870.1025
Classification Product Code: MHX
Date Received: 12/14/2010
Decision Date: 01/07/2011
Regulation Medical Specialty: Cardiovascular
Device Name: INTELLIVUE MX40 PATIENT MONITOR
Manufacturer: PHILLIPS MEDICAL SYSTEMS
Device Classification Name: monitor, physiological, patient(with arrhythmia detection or alarms)
Regulation Number: 870.1025
Classification Product Code: MHX
Date Received: 12/14/2010
Decision Date: 01/07/2011
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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