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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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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 FEI # 2431353
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 FEI # 2431353
Non-Invasive Monitoring Systems, Inc.
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