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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K080251
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Recall
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FDA Recall
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GE Healthcare, ApexPro Telemetry System The ApexPro Telemetry System is intended for use under the... 2 03/03/2011 FEI # 2126677
GE Healthcare, LLC
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