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FDA 510(k), K070069, ZIPPREP ELECTRODE
FDA 510(k), K070069, ZIPPREP ELECTRODE
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510(K) Number: K070069
Device Name: ZIPPREP ELECTRODE
Manufacturer: VIKRAM VERMA
Device Classification Name: Electrode, Cutaneous
Regulation Number: GXY
Classification Product Code: 01/08/2007
Date Received: 02/05/2007
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: ZIPPREP ELECTRODE
Manufacturer: VIKRAM VERMA
Device Classification Name: Electrode, Cutaneous
Regulation Number: GXY
Classification Product Code: 01/08/2007
Date Received: 02/05/2007
Decision Date: Substantially Equivalent (SESE)
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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