Medical Device Recalls
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1 result found
510(K) Number: K002159 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart ... | 2 | 07/11/2013 | SagaTech Electronics, Inc. |
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