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U.S. Department of Health and Human Services

Medical Device Recalls

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510(K) Number: K010925
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Ventilator System Servo-i V3.1 Maquet Critical Care PC1771 2 02/10/2007 MAQUET Inc.
Ventilator System SERVO-i V3.1 PC1777 Maquet Critical Care 2 01/25/2007 MAQUET Inc.
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