FDA 510(k), K984053, BECKER EXTERNAL DRAINAGE AND MONITORING SYSTEM

FDA 510(k), K984053, BECKER EXTERNAL DRAINAGE AND MONITORING SYSTEM

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510(K) Number: K984053
Device Name: BECKER EXTERNAL DRAINAGE AND MONITORING SYSTEM
Manufacturer:
Device Classification Name: Shunt, Central Nervous System And Components
Regulation Number: 882.5550
Classification Product Code: JXG
Date Received: 11/06/1998
Decision Date: 02/04/1999
Regulation Medical Specialty: Neurology
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