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FDA 510(k), K970587, AD-TECH SUBDURAL ELECTRODE
FDA 510(k), K970587, AD-TECH SUBDURAL ELECTRODE
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510(K) Number: K970587
Device Name: AD-TECH SUBDURAL ELECTRODE
Manufacturer: AD-TECH MEDICAL INSTRUMENT CORP.
Device Classification Name: electrode, cortical
Regulation Number: 882.1310
Classification Product Code: GYC
Date Received: 02/18/1997
Decision Date: 05/09/1997
Regulation Medical Specialty: Neurology
Device Name: AD-TECH SUBDURAL ELECTRODE
Manufacturer: AD-TECH MEDICAL INSTRUMENT CORP.
Device Classification Name: electrode, cortical
Regulation Number: 882.1310
Classification Product Code: GYC
Date Received: 02/18/1997
Decision Date: 05/09/1997
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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