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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: K121424
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Product Description
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Recall
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FDA Recall
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Invivo Corporation Expression Information Portal (Model IP5) is intended to be used as a secondary d... 2 02/14/2014 FEI # 1051786
Invivo Corporation
Invivo Corporation Expression IP5 Information Portal Product Usage: The Expression Informati... 2 02/26/2014 FEI # 1051786
Invivo Corporation
Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and devic... 2 08/19/2014 FEI # 1051786
Invivo Corporation
Philips Expression Information Portal (IP5) Model 865471. The IP5 is intended to be used as a seco... 2 09/21/2016 FEI # 1051786
Invivo Corporation
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