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FDA 510(k), K023351, MAGIC INFUSION CATHETER
FDA 510(k), K023351, MAGIC INFUSION CATHETER
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510(K) Number: K023351
Device Name: MAGIC INFUSION CATHETER
Manufacturer: ADVANCED INTERVENTIONAL TECHNOLOGIES, LLC
Device Classification Name: catheter, continuous flush
Regulation Number: 870.1210
Classification Product Code: KRA
Date Received: 10/07/2002
Decision Date: 02/20/2003
Regulation Medical Specialty: Cardiovascular
Device Name: MAGIC INFUSION CATHETER
Manufacturer: ADVANCED INTERVENTIONAL TECHNOLOGIES, LLC
Device Classification Name: catheter, continuous flush
Regulation Number: 870.1210
Classification Product Code: KRA
Date Received: 10/07/2002
Decision Date: 02/20/2003
Regulation Medical Specialty: Cardiovascular
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