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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K072507
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Product Description
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Recall
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FDA Recall
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EKOS EndoWave Infusion System consisting of a Drug Delivery Catheter and an Ultrasound Core. Labele... 2 09/16/2008 EKOS Corporation
PT-3B Control Unit - component of the EndoWave Infusion Catheter System. EndoWave Infusion System c... 2 09/02/2008 EKOS Corporation
Infusion System. EKOS EndoWave Infusion System. EKOS EndoWave Infusion System Drug Delivery Catheter... 2 08/20/2008 EKOS Corporation
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