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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K932645
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FDA Recall
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Gyroscan ACS-NT system 2 09/12/2003 Philips Medical Systems
Gyroscan ACS-NT with software versions R6x, R7x, R8x 2 09/12/2003 Philips Medical Systems
Gyroscan Intera 1.0T & 1.5T 2 09/12/2003 Philips Medical Systems
Gyroscan NT-Intera 2 09/12/2003 Philips Medical Systems
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