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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K122821
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Product Description
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FDA Recall
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CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage: The CELLTRACKS AUTO... 2 08/10/2013 FEI # 3004619490
Veridex, LLC
CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage: The CELLTRACKS AUTOPREP... 2 08/10/2013 FEI # 3004619490
Veridex, LLC
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