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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: KXA
Date Received: 10/05/1979
Decision Date: 01/16/1980
Decision: 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: KXA
Date Received: 10/05/1979
Decision Date: 01/16/1980
Decision: Substantially Equivalent (SESE)
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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