Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Z-1820-2012 - USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device,... | 2 | 06/18/2012 | Non-Invasive Monitoring Systems, Inc. |
Z-1819-2012 - US-001 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, ... | 2 | 06/18/2012 | Non-Invasive Monitoring Systems, Inc. |
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