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FDA 510(k), K964644, AD-TECH'S DEPTH ELECTRODE
FDA 510(k), K964644, AD-TECH'S DEPTH ELECTRODE
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510(K) Number: K964644
Device Name: AD-TECH'S DEPTH ELECTRODE
Manufacturer: AD-TECH MEDICAL INSTRUMENT CORP.
Device Classification Name: electrode, depth
Regulation Number: 882.1330
Classification Product Code: GZL
Date Received: 10/31/1996
Decision Date: 05/09/1997
Regulation Medical Specialty: Neurology
Device Name: AD-TECH'S DEPTH ELECTRODE
Manufacturer: AD-TECH MEDICAL INSTRUMENT CORP.
Device Classification Name: electrode, depth
Regulation Number: 882.1330
Classification Product Code: GZL
Date Received: 10/31/1996
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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