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FDA 510(k), K792007, CSF-VENTRICULAR CATHETER, STANDARD DES
FDA 510(k), K792007, CSF-VENTRICULAR CATHETER, STANDARD DES
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510(K) Number: K792007
Device Name: CSF-VENTRICULAR CATHETER, STANDARD DES
Manufacturer:
Device Classification Name: Shunt, Central Nervous System And Components
Regulation Number: JXG
Classification Product Code: 10/05/1979
Date Received: 01/16/1980
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: CSF-VENTRICULAR CATHETER, STANDARD DES
Manufacturer:
Device Classification Name: Shunt, Central Nervous System And Components
Regulation Number: JXG
Classification Product Code: 10/05/1979
Date Received: 01/16/1980
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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