FDA 510(k), K983454, PAIN CARE 2000

FDA 510(k), K983454, PAIN CARE 2000

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510(K) Number: K983454
Device Name: PAIN CARE 2000
Manufacturer:
Device Classification Name: Pump, Infusion, Elastomeric
Regulation Number: 880.5725
Classification Product Code: MEB
Date Received: 09/30/1998
Decision Date: 12/16/1998
Regulation Medical Specialty: General Hospital
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