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FDA 510(k), K050702, NEUROSYSTEMS 1TM MONITOR
FDA 510(k), K050702, NEUROSYSTEMS 1TM MONITOR
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510(K) Number: K050702
Device Name: NEUROSYSTEMS 1TM MONITOR
Manufacturer: NEUROSYSTEMS LLC
Device Classification Name: device, monitoring, intracranial pressure
Regulation Number: 882.1620
Classification Product Code: GWM
Date Received: 03/18/2005
Decision Date: 05/17/2005
Regulation Medical Specialty: Neurology
Device Name: NEUROSYSTEMS 1TM MONITOR
Manufacturer: NEUROSYSTEMS LLC
Device Classification Name: device, monitoring, intracranial pressure
Regulation Number: 882.1620
Classification Product Code: GWM
Date Received: 03/18/2005
Decision Date: 05/17/2005
Regulation Medical Specialty: Neurology
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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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