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FDA 510(k), K021185, NERVUS MONITOR
FDA 510(k), K021185, NERVUS MONITOR
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510(K) Number: K021185
Device Name: NERVUS MONITOR
Manufacturer: TAUGAGREINING HF
Device Classification Name: standard polysomnograph with electroencephalograph
Regulation Number: 882.1400
Classification Product Code: OLV
Date Received: 04/15/2002
Decision Date: 07/12/2002
Regulation Medical Specialty: Neurology
Device Name: NERVUS MONITOR
Manufacturer: TAUGAGREINING HF
Device Classification Name: standard polysomnograph with electroencephalograph
Regulation Number: 882.1400
Classification Product Code: OLV
Date Received: 04/15/2002
Decision Date: 07/12/2002
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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