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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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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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